Fiala, Tomas’s team published research in Journal of the American Chemical Society in 2020 | CAS: 14660-52-7

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Quality Control of Ethyl 5-bromovalerate

《Chemical Targeting of Voltage Sensitive Dyes to Specific Cells and Molecules in the Brain》 was written by Fiala, Tomas; Wang, Jihang; Dunn, Matthew; Sebej, Peter; Choi, Se Joon; Nwadibia, Ekeoma C.; Fialova, Eva; Martinez, Diana M.; Cheetham, Claire E.; Fogle, Keri J.; Palladino, Michael J.; Freyberg, Zachary; Sulzer, David; Sames, Dalibor. Quality Control of Ethyl 5-bromovalerateThis research focused onvoltage sensitive fluorescent dye brain. The article conveys some information:

Voltage sensitive fluorescent dyes (VSDs) are important tools for probing signal transduction in neurons and other excitable cells. The impact of these highly lipophilic sensors has, however, been limited due to the lack of cell-specific targeting methods in brain tissue or living animals. The authors address this key challenge by introducing a nongenetic mol. platform for cell- and mol.-specific targeting of synthetic VSDs in the brain. The authors employ a dextran polymer particle to overcome the inherent lipophilicity of VSDs by dynamic encapsulation and high-affinity ligands to target the construct to specific neuronal cells utilizing only native components of the neurotransmission machinery at physiol. expression levels. Dichloropane, a monoamine transporter ligand, enables targeting of dense dopaminergic axons in the mouse striatum and sparse noradrenergic axons in the mouse cortex in acute brain slices. PFQX in conjunction with ligand-directed acyl imidazole chem. enables covalent labeling of AMPA-type glutamate receptors in the same brain regions. Probe variants bearing either a classical electrochromic ANEP dye or state-of-the-art VoltageFluor-type dye respond to membrane potential changes in a similar manner to the parent dyes, as shown by whole-cell patch recording. The authors demonstrate the feasibility of optical voltage recording with the probes in brain tissue with one-photon and two-photon fluorescence microscopy and define the signal limits of optical voltage imaging with synthetic sensors under a low photon budget determined by the native expression levels of the target proteins. This work demonstrates the feasibility of a chem. targeting approach and expands the possibilities of cell-specific imaging and pharmacol. After reading the article, we found that the author used Ethyl 5-bromovalerate(cas: 14660-52-7Quality Control of Ethyl 5-bromovalerate)

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Quality Control of Ethyl 5-bromovalerate

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Duan, Honghong’s team published research in Angewandte Chemie, International Edition in 2020 | CAS: 623-24-5

1,4-Bis(bromomethyl)benzene(cas: 623-24-5) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Quality Control of 1,4-Bis(bromomethyl)benzene Alkyl bromides are mainly used as alkylating agents and also find application as a solvent to extract oil from seeds and wool.

Quality Control of 1,4-Bis(bromomethyl)benzeneIn 2020 ,《Host-Guest Recognition and Fluorescence of a Tetraphenylethene-Based Octacationic Cage》 was published in Angewandte Chemie, International Edition. The article was written by Duan, Honghong; Li, Yawen; Li, Qingfang; Wang, Pinpin; Liu, Xueru; Cheng, Lin; Yu, Yang; Cao, Liping. The article contains the following contents:

We report the synthesis and characterization of a three-dimensional tetraphenylethene-based octacationic cage that shows host-guest recognition of polycyclic aromatic hydrocarbons (e.g. coronene) in organic media and water-soluble dyes (e.g. sulforhodamine 101) in aqueous media through CH···π, π-π, and/or electrostatic interactions. The cage⊃coronene exhibits a cuboid internal cavity with a size of approx. 17.2×11.0x6.96 Å3 and a “”hamburger””-type host-guest complex, which is hierarchically stacked into 1D nanotubes and a 3D supramol. framework. The free cage possesses a similar cavity in the crystalline state. Furthermore, a host-guest complex formed between the octacationic cage and sulforhodamine 101 had a higher absolute quantum yield (φF=28.5%), larger excitation-emission gap (Δλex-em=211 nm), and longer emission lifetime (τ=7.0 ns) as compared to the guest (φF=10.5%; Δλex-em=11 nm; τ=4.9 ns), and purer emission (ΔλFWHM=38 nm) as compared to the host (ΔλFWHM=111 nm). In the experiment, the researchers used many compounds, for example, 1,4-Bis(bromomethyl)benzene(cas: 623-24-5Quality Control of 1,4-Bis(bromomethyl)benzene)

1,4-Bis(bromomethyl)benzene(cas: 623-24-5) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Quality Control of 1,4-Bis(bromomethyl)benzene Alkyl bromides are mainly used as alkylating agents and also find application as a solvent to extract oil from seeds and wool.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Zhang, Minghao’s team published research in Angewandte Chemie, International Edition in 2020 | CAS: 402-43-7

1-Bromo-4-(trifluoromethyl)benzene(cas: 402-43-7) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. HPLC of Formula: 402-43-7

HPLC of Formula: 402-43-7In 2020 ,《Divergent and Stereoselective Synthesis of Tetraarylethylenes from Vinylboronates》 was published in Angewandte Chemie, International Edition. The article was written by Zhang, Minghao; Yao, Yisen; Stang, Peter J.; Zhao, Wanxiang. The article contains the following contents:

The synthesis of a new tetraborylethylene (TBE) is reported, and its application in the preparation of [4+0]-tetraarylethenes (TAEs) is elucidated. TAEs have widespread applications in material science and supramol. chem. due to their aggregation-induced emission (AIE) properties. The divergent and stereoselective synthesis of [3+1]-, [2+2]-, and [2+1+1]-TAEs via multiple couplings of vinylboronates with aryl bromides is demonstrated. These couplings feature a broad substrate scope and excellent functional group compatibility due to mild reaction conditions. Facile access to various tetraarylethenes is provided. This strategy represents an important complement to the conventional methods employed for the synthesis of TAEs, and would be a valuable tool for synthesizing TAE-based mols. useful in functional materials, biol. imaging and chem. sensing. In the experimental materials used by the author, we found 1-Bromo-4-(trifluoromethyl)benzene(cas: 402-43-7HPLC of Formula: 402-43-7)

1-Bromo-4-(trifluoromethyl)benzene(cas: 402-43-7) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. HPLC of Formula: 402-43-7

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Kondo, Masaki’s team published research in Angewandte Chemie, International Edition in 2020 | CAS: 1129-28-8

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Alkyl bromides are mainly used as alkylating agents and also find application as a solvent to extract oil from seeds and wool. Safety of Methyl 3-(bromomethyl)benzoate

Safety of Methyl 3-(bromomethyl)benzoateIn 2020 ,《Silaboration of [1.1.1]Propellane: A Storable Feedstock for Bicyclo[1.1.1]pentane Derivatives》 was published in Angewandte Chemie, International Edition. The article was written by Kondo, Masaki; Kanazawa, Junichiro; Ichikawa, Tomohiro; Shimokawa, Takumi; Nagashima, Yuki; Miyamoto, Kazunori; Uchiyama, Masanobu. The article contains the following contents:

The silaboration of [1.1.1]propellane enables direct introduction of B and Si functional groups onto the bicyclo[1.1.1]pentane (BCP) scaffold in high yield under mild, additive-free conditions. The silaborated BCP can be obtained on a gram-scale in a single step without the need for column-chromatog. purification, and is storable and easy to handle, providing a versatile synthetic intermediate for BCP derivatives We also describe various conversions of the C-B/C-Si bonds on the BCP scaffold, including development of a modified Suzuki-Miyaura cross-coupling reaction at the highly sterically hindered bridgehead sp3 carbon center of the BCP skeleton using a combination of highly activated BCP boronic esters, copper(I) oxide, and a PdCl2(dppf) catalyst system. In the experiment, the researchers used many compounds, for example, Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8Safety of Methyl 3-(bromomethyl)benzoate)

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Alkyl bromides are mainly used as alkylating agents and also find application as a solvent to extract oil from seeds and wool. Safety of Methyl 3-(bromomethyl)benzoate

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Xie, Yun-Dong’s team published research in Bioorganic & Medicinal Chemistry Letters in 2021 | CAS: 14660-52-7

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents.Recommanded Product: Ethyl 5-bromovalerate

Xie, Yun-Dong; Xu, Yan-Hong; Liu, Ji-Ping; Wang, Bin; Shi, Yong-Heng; Wang, Wei; Wang, Xiao-Ping; Sun, Meng; Xu, Xin-Ya; Bian, Xiao-Li published their research in Bioorganic & Medicinal Chemistry Letters in 2021. The article was titled 《1,3-Benzodioxole-based fibrate derivatives as potential hypolipidemic and hepatoprotective agents》.Recommanded Product: Ethyl 5-bromovalerate The article contains the following contents:

A series of target compounds 1,3-benzodioxole-based fibrate derivatives were designed and synthesized. All the target compounds were preliminarily evaluated by hyperlipidemia mice induced by Triton WR-1339, in which compound I displayed a greater anti-hyperlipidemia activity than other compounds as well as pos. drug fenofibrate (FF). I showed a significant reduction of plasma lipids, such as triglycerides (TG), total cholesterol (TC) and low-d. lipoprotein cholesterin (LDL-C), in high fat diet (HFD) induced hyperlipidemic mice. In addition, hepatic transaminases (AST and ALT) were ameliorated after administration of I, in particular the AST, and the histopathol. examination showed that I improved the hepatic lipid accumulation. The expression of PPAR-α involved in lipids metabolism was up-regulated in the liver tissues of 12-treated group. Other significant activity such as antioxidant, and anti-inflammation was confirmed and reinforced the effects of I as a potential hypolipidemia and hepatoprotective agent.Ethyl 5-bromovalerate(cas: 14660-52-7Recommanded Product: Ethyl 5-bromovalerate) was used in this study.

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents.Recommanded Product: Ethyl 5-bromovalerate

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Schaeker-Huebner, Linda’s team published research in Journal of Medicinal Chemistry in 2021 | CAS: 17696-11-6

8-Bromooctanoic acid(cas: 17696-11-6) acid is used in the synthesis of 8-(N-Methyl-4,4′-bipyridinyl)- octanoic acid. 8-Mercaptooctanoic acid was prepared from 8-bromooctanoic acid. And 8-Bromooctanoic Acid is a useful compound for sonodynamic therapy.SDS of cas: 17696-11-6

Schaeker-Huebner, Linda; Warstat, Robin; Ahlert, Heinz; Mishra, Pankaj; Kraft, Fabian B.; Schliehe-Diecks, Julian; Schoeler, Andrea; Borkhardt, Arndt; Breit, Bernhard; Bhatia, Sanil; Huegle, Martin; Guenther, Stefan; Hansen, Finn K. published their research in Journal of Medicinal Chemistry in 2021. The article was titled 《4-Acyl Pyrrole Capped HDAC Inhibitors: A New Scaffold for Hybrid Inhibitors of BET Proteins and Histone Deacetylases as Antileukemia Drug Leads》.SDS of cas: 17696-11-6 The article contains the following contents:

Multitarget drugs are an emerging alternative to combination therapies. In three iterative cycles of design, synthesis, and biol. evaluation, we developed a novel type of potent hybrid inhibitors of bromodomain, and extra-terminal (BET) proteins and histone deacetylases (HDACs) based on the BET inhibitor XD14 and well-established HDAC inhibitors. The most promising new hybrids, 49 and 61, displayed submicromolar inhibitory activity against HDAC1-3 and 6, and BRD4(1), and possess potent antileukemia activity. 49 induced apoptosis more effectively than the combination of ricolinostat and birabresib (1:1). The most balanced dual inhibitor, 61, induced significantly more apoptosis than the related control compounds 62 (no BRD4(1) affinity) and 63 (no HDAC inhibition) as well as the 1:1 combination of both. Addnl., 61 (I) was well tolerated in an in vivo zebrafish toxicity model. Overall, our data suggest an advantage of dual HDAC/BET inhibitors over the combination of two single targeted compounds In the experiment, the researchers used 8-Bromooctanoic acid(cas: 17696-11-6SDS of cas: 17696-11-6)

8-Bromooctanoic acid(cas: 17696-11-6) acid is used in the synthesis of 8-(N-Methyl-4,4′-bipyridinyl)- octanoic acid. 8-Mercaptooctanoic acid was prepared from 8-bromooctanoic acid. And 8-Bromooctanoic Acid is a useful compound for sonodynamic therapy.SDS of cas: 17696-11-6

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Singh, Sarita’s team published research in Bioorganic & Medicinal Chemistry Letters in 2020 | CAS: 14660-52-7

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact.COA of Formula: C7H13BrO2

《Synthesis and evaluation of substituted 8,8-dimethyl-8H-pyrano[2,3-f]chromen-2-one derivatives as vasorelaxing agents》 was published in Bioorganic & Medicinal Chemistry Letters in 2020. These research results belong to Singh, Sarita; Agarwal, Karishma; Iqbal, Hina; Yadav, Pankaj; Yadav, Deepika; Chanda, Debabrata; Tandon, Sudeep; Khan, Feroz; Gupta, Anil Kumar; Gupta, Atul. COA of Formula: C7H13BrO2 The article mentions the following:

A series of substituted 8,8-dimethyl-8H-pyrano[2,3-f]chromen-2-ones I [R = Me, (CH2)2NMe2, CH2C(O)N(Me)(n-Bu), etc.] was synthesized from scopoletin as vasorelaxing agents. The synthesized compounds were evaluated for vasorelaxation in endothelium intact rat main mesenteric artery (MMA). Scopoletin, and compounds I [R = Me, CH2C(O)N(Me)(n-Bu), (CH2)4C(O)N(Me)(n-Bu), CH2C(O)NH(n-pentyl), (CH2)3C(O)N(Me)(n-pentyl), (CH2)4C(O)NH(n-pentyl)] showed significant vasorelaxation in precontracted MMA within the range of EC50 value 1.58-5.02μM. These derivatives presented 29.40-70.89 fold increased sensitivity for exptl. tissue compared to scopoletin, the parent mol. Among others, compound I [R = Me] was found to be the most active compound which had EC50 1.58μM with 70.89 fold increased sensitivity. The mechanistic evaluation of compound I [R = Me] showed that it exerted vasorelaxation through Ca2+-activated K+ (BKca) channel and the effect was endothelium-independent. In the experimental materials used by the author, we found Ethyl 5-bromovalerate(cas: 14660-52-7COA of Formula: C7H13BrO2)

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact.COA of Formula: C7H13BrO2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Van der Maelen, Juan F.’s team published research in Journal of Molecular Structure in 2020 | CAS: 14516-54-2

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Application of 14516-54-2

《Two octahedral σ-borane metal (MnI and RuII) complexes containing a tripod κ3N,H,H-ligand: Synthesis, structural characterization, and theoretical topological study of the charge density》 was published in Journal of Molecular Structure in 2020. These research results belong to Van der Maelen, Juan F.; Brugos, Javier; Garcia-Alvarez, Pablo; Cabeza, Javier A.. Application of 14516-54-2 The article mentions the following:

Theor. electron d. (QTAIM) studies in the gas-phase have shown that the attachment of the BH3 group to the metal atom in complexes [Mn(κ3N,H,H-iPr2bzamBH3)(CO)3] (1) and [Ru(η5-C5Me5)(κ3N,H,H-iPr2bzamBH3)] (2) (HiPr2bzamBH3 = N-trihydridoborane-N,N’-bis(isopropyl) benzamidine) is sym. in the latter but asym. in the former, and involves two B-H-metal interactions that are intermediate between κ1H (Shimoi type) and κ2H,B (agostic type). The herein reported results, coupled to previous ones on related complexes having a similar tripod κ3N,H,H-borane ligand, show that the bonding similarities and differences within each particular M(μ-H)2B moiety are not related to the type of metal atom, nor even to its coordination geometry, but mainly to the mol. symmetry. In addition to this study using Bromopentacarbonylmanganese(I), there are many other studies that have used Bromopentacarbonylmanganese(I)(cas: 14516-54-2Application of 14516-54-2) was used in this study.

Bromopentacarbonylmanganese(I)(cas: 14516-54-2) has many other uses. It is used in the formation of (eta6-arene)tricarbonylmanganese(I) by reacting with arene (arene= hexamethyl benzene, 1,2,4,5-tetramethyl benzene, mesitylene, p-xylene and toluene) in the presence silver salt.Application of 14516-54-2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Zhu, Tianhao’s team published research in Industrial & Engineering Chemistry Research in 2021 | CAS: 623-24-5

1,4-Bis(bromomethyl)benzene(cas: 623-24-5) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Due to the reactivity of bromide, they are used as potential precursors or important intermediates in organic synthesis. Recommanded Product: 1,4-Bis(bromomethyl)benzene

Recommanded Product: 1,4-Bis(bromomethyl)benzeneIn 2021 ,《Highly Proton Conductive Phosphoric Acid Porous Organic Polymers via Knitting Method》 appeared in Industrial & Engineering Chemistry Research. The author of the article were Zhu, Tianhao; Shi, Benbing; Wu, Hong; You, Xinda; Wang, Xiaoyao; Fan, Chunyang; Peng, Quan; Jiang, Zhongyi. The article conveys some information:

Phosphoric acid group, which possesses a low energy barrier for proton conduction and high water bonding energy, favors proton conduction and water retention. In this study, a phosphoric acid porous organic polymer (PAPOP) with high proton conductivity was synthesized. The di-Et benzylphosphonate (DBP) monomer and the benzyl monomer were directly knitted via the Friedel-Crafts alkylation reaction to form a porous scaffold. The phosphate ester group on DBP not only enhanced the monomer reactivity but also realized the in situ introduction of the phosphoric acid group precursor during the formation of the porous scaffold. It is found that p-dichloroxylene (DCX) monomer, due to its higher electrophilic activity, is easier to react with DBP and thus easier to introduce phosphoric acid groups. The higher ratio of DCX leads to a more continuous hydrogen-bond network within the scaffold, which facilitates the proton-conducting process. The resultant porous organic polymers exhibited high hydrophilicity and excellent stability in strong acid as well as antiswelling ability in water. The highest ion-exchange capacity reached 2.68 mmol g-1, much higher than that of most reported polymers. The proton conductivity of powders reached the highest value of 7.09 × 10-2 S cm-1 at 348 K and 98% relative humidity. In addition to this study using 1,4-Bis(bromomethyl)benzene, there are many other studies that have used 1,4-Bis(bromomethyl)benzene(cas: 623-24-5Recommanded Product: 1,4-Bis(bromomethyl)benzene) was used in this study.

1,4-Bis(bromomethyl)benzene(cas: 623-24-5) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Due to the reactivity of bromide, they are used as potential precursors or important intermediates in organic synthesis. Recommanded Product: 1,4-Bis(bromomethyl)benzene

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Krogsgaard-Larsen, Niels’s team published research in Journal of Medicinal Chemistry in 2017 | CAS: 1129-28-8

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.Organobromine chemicals are produced naturally by an array of biological and other chemical processes in our environment. Organobromine compounds are produced naturally by marine creatures (sponges, corals, sea slugs, tunicates, sea fans) and seaweed, plants, fungi, lichen, algae, bacteria, microbes, and some mammals. Reference of Methyl 3-(bromomethyl)benzoate

Reference of Methyl 3-(bromomethyl)benzoateIn 2017 ,《Design and synthesis of a series of L-trans-4-substituted prolines as selective antagonists for the ionotropic glutamate receptors including functional and X-ray crystallographic studies of new subtype selective kainic acid receptor subtype 1 (Gluk1) antagonist (2S,4R)-4-(2-carboxyphenoxy)pyrrolidine-2-carboxylic acid》 appeared in Journal of Medicinal Chemistry. The author of the article were Krogsgaard-Larsen, Niels; Delgar, Claudia G.; Koch, Karina; Brown, Patricia M. G. E.; Moeller, Charlotte; Han, Liwei; Huynh, Tri H. V.; Hansen, Stinne W.; Nielsen, Birgitte; Bowie, Derek; Pickering, Darryl S.; Kastrup, Jette Sandholm; Frydenvang, Karla; Bunch, Lennart. The article conveys some information:

Ionotropic glutamate receptor antagonists are valuable tool compounds for studies of neurol. pathways in the central nervous system. On the basis of rational ligand design, a new class of selective antagonists, represented by (2S,4R)-4-(2-carboxyphenoxy)pyrrolidine-2-carboxylic acid (I), for cloned homomeric kainic acid receptors subtype 1 (GluK1) was attained (Ki = 4 μM). In a functional assay, I displayed full antagonist activity with IC50 = 6 ± 2 μM. A crystal structure was obtained of I when bound in the ligand binding domain of GluK1. A domain opening of 13-14° was seen compared to the structure with glutamate, consistent with I being an antagonist. A structure-activity relationship study showed that the chem. nature of the tethering atom (C, O, or S) linking the pyrrolidine ring and the Ph ring plays a key role in the receptor selectivity profile and that substituents on the Ph ring are well accommodated by the GluK1 receptor. The experimental process involved the reaction of Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8Reference of Methyl 3-(bromomethyl)benzoate)

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.Organobromine chemicals are produced naturally by an array of biological and other chemical processes in our environment. Organobromine compounds are produced naturally by marine creatures (sponges, corals, sea slugs, tunicates, sea fans) and seaweed, plants, fungi, lichen, algae, bacteria, microbes, and some mammals. Reference of Methyl 3-(bromomethyl)benzoate

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary