Zhu, Xuezhen’s team published research in Journal of Medicinal Chemistry in 2019 | CAS: 1129-28-8

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.Most of the natural organobromine compounds are produced by marine organisms , and several brominated metabolites with antibacterial , antitumor , antiviral , and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. Related Products of 1129-28-8 In contrast, terrestrial plants account only for a few bromine-containing compounds.

《Triazole Bridged Flavonoid Dimers as Potent, Nontoxic, and Highly Selective Breast Cancer Resistance Protein (BCRP/ABCG2) Inhibitors》 was written by Zhu, Xuezhen; Wong, Iris L. K.; Chan, Kin-Fai; Cui, Jiahua; Law, Man Chun; Chong, Tsz Cheung; Hu, Xuesen; Chow, Larry M. C.; Chan, Tak Hang. Related Products of 1129-28-8This research focused ontriazole bridged flavonoid dimer breast cancer SAR docking. The article conveys some information:

The present work describes the syntheses of diverse triazole bridged flavonoid dimers and identifies potent, nontoxic, and highly selective BCRP inhibitors. A homodimer, Ac22(Az8)2, with m-methoxycarbonylbenzyloxy substitution at C-3 of the flavone moieties and a bis-triazole-containing linker (21 atoms between the two flavones) showed low toxicity (IC50 toward L929, 3T3, and HFF-1 > 100 μM), potent BCRP-inhibitory activity (EC50 = 1-2 nM), and high BCRP selectivity (BCRP selectivity over MRP1 and P-gp > 455-909). Ac22(Az8)2 inhibits BCRP-ATPase activity, blocks the drug efflux activity of BCRP, elevates the intracellular drug accumulation, and finally restores the drug sensitivity of BCRP-overexpressing cells. It does not down-regulate the surface BCRP protein expression to enhance the drug retention. Therefore, Ac22(Az8)2 and similar flavonoid dimers appear to be promising candidates for further development into combination therapy to overcome MDR cancers with BCRP overexpression. In the experimental materials used by the author, we found Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8Related Products of 1129-28-8)

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.Most of the natural organobromine compounds are produced by marine organisms , and several brominated metabolites with antibacterial , antitumor , antiviral , and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. Related Products of 1129-28-8 In contrast, terrestrial plants account only for a few bromine-containing compounds.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Abdul Rub, Malik’s team published research in Colloid and Polymer Science in 2019 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Formula: C6H12Br2

《Interaction of ninhydrin with zinc(II) complex of tryptophan in the three dicationic gemini surfactants》 was written by Abdul Rub, Malik; Kumar, Dileep. Formula: C6H12Br2This research focused onzinc ninhydrin tryptophan gemini surfactant critical micellar concentration. The article conveys some information:

Present work concerns with the interaction of ninhydrin with zinc(II) complex of tryptophan ([Zn(II)-Trp]+) in the three dicationic gemini surfactant systems. To record critical micellar concentration (CMC) and absorbance, we have used Systronics conductivity meter and UV-visible spectrophotometer, resp. Experiment opens up the fractional- and first-order paths in ninhydrin and complex, resp. Gemini micellar medium is found more superior over aqueous medium. Rate constant (kψ) vs. [gemini] plot shows the unusual role of geminis on kψ. kψ increases with gemini concentration (at concentrations lower than the CMC, part I) and leveling-off regions obtain (concentration up to 400 × 10-5 mol dm-3, part II). Characteristics of part I and part II are just the same as that of conventional surfactant. Later, gemini produces a third region of increasing kψ at higher concentrations ([gemini] > 400 × 10-5 mol dm-3, part III). Detail and systematic elucidation about the effect of surfactants are mentioned and discussed in the text. Binding constants (KS for [Zn(II)-Trp]+ and KN for ninhydrin) and rate constant (km in geminis) were determined by nonlinear least squares regression technique. The kinetic results acquired can reasonably be interpreted by pseudo-phase model of surfactant micelles. In the experimental materials used by the author, we found 1,6-Dibromohexane(cas: 629-03-8Formula: C6H12Br2)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Formula: C6H12Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Kim, Seon-Mi’s team published research in Journal of Medicinal Chemistry in 2016 | 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. Due to the reactivity of bromide, they are used as potential precursors or important intermediates in organic synthesis. Application In Synthesis of Methyl 3-(bromomethyl)benzoate

《Discovery of an Orally Bioavailable Gonadotropin-Releasing Hormone Receptor Antagonist》 was written by Kim, Seon-Mi; Lee, Minhee; Lee, So Young; Park, Euisun; Lee, Soo-Min; Kim, Eun Jeong; Han, Min Young; Yoo, Taekyung; Ann, Jihyae; Yoon, Suyoung; Lee, Jiyoun; Lee, Jeewoo. Application In Synthesis of Methyl 3-(bromomethyl)benzoateThis research focused onuracil derivative SKI2496 preparation GnRH receptor antagonist pharmacokinetics. The article conveys some information:

The authors developed a compound library for orally available gonadotropin-releasing hormone (GnRH) receptor antagonists that were based on a uracil scaffold. Based on in vitro activity and CYP inhibition profile, the authors selected 18a ((R)-4-((2-(3-(2-fluoro-6-(trifluoromethyl)benzyl)-4-methyl-2,6-dioxo-5-(4-((5-(trifluoromethyl)-furan-2-yl)methyl)-piperazin-1-yl)-2,3-dihydropyrimidin-1(6H)-yl)-1-phenylethyl)-amino)-butanoic acid, SKI2496) for further in vivo studies. Compound 18a exhibited more selective antagonistic activity toward the human GnRH receptors over the GnRHRs in monkeys and rats, and this compound also showed inhibitory effects on GnRH-mediated signaling pathways. Pharmacokinetic and pharmacodynamic evaluations of 18a revealed improved bioavailability and superior gonadotropic suppression activity compared with Elagolix, the most clin. advanced compound Considering that 18a exhibited highly potent and selective antagonistic activity toward the hGnRHRs along with favorable pharmacokinetic profiles, the authors believe that 18a may represent a promising candidate for an orally available hormonal therapy. The experimental process involved the reaction of Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8Application In Synthesis 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. Due to the reactivity of bromide, they are used as potential precursors or important intermediates in organic synthesis. Application In Synthesis of Methyl 3-(bromomethyl)benzoate

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Gan, Shaolin’s team published research in Catalysis Science & Technology in 2022 | CAS: 3141-27-3

2,5-Dibromothiophene(cas: 3141-27-3) , is mainly used as pharmaceutical intermediate and synthesis intermediate. 2,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) .Synthetic Route of C4H2Br2S

《Click-based conjugated microporous polymers as efficient heterogeneous photocatalysts for organic transformations》 was written by Gan, Shaolin; Zeng, Yan; Liu, Jiaxin; Nie, Junqi; Lu, Cuifen; Ma, Chao; Wang, Feiyi; Yang, Guichun. Synthetic Route of C4H2Br2SThis research focused ontriazole thiophene conjugated polymer catalyst preparation optical band gap; dimethylaniline aryl iso isocyanide triazolethiophene catalyst ugi reaction; methyl arylamino phenylacetanmide preparation; tetrahydroisoquinoline triazolethiophene catalyst oxidation; tetrahydroisoquinolinone preparation. The article conveys some information:

In this study, the design and synthesis of three 1,2,3-triazole-thiophene based CMP (Ta-Th) photocatalysts through the click reaction was described. Compared with the corresponding thienyl- and bithienyl-bridged Ta-Th-4 and Ta-Th-5, the terthiophene based Ta-Th-6 shows a stronger light-harvesting ability, a narrower optical energy gap, and a better charge separation efficiency for facilitated charge transfer, which make Ta-Th-6 a promising candidate for photoredox reactions. Indeed, Ta-Th-6 presents superior photocatalytic activity in the Ugi multicomponent reaction and α-oxidation of N-substituted tetrahydroisoquinolines. Furthermore, the catalyst exhibits a considerable activity after recycling five times, demonstrating its high stability and excellent reusability. The experimental part of the paper was very detailed, including the reaction process of 2,5-Dibromothiophene(cas: 3141-27-3Synthetic Route of C4H2Br2S)

2,5-Dibromothiophene(cas: 3141-27-3) , is mainly used as pharmaceutical intermediate and synthesis intermediate. 2,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) .Synthetic Route of C4H2Br2S

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Lin, Rui-Lian’s team published research in Journal of Organic Chemistry in 2020 | 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.Recommanded Product: 17696-11-6

Recommanded Product: 17696-11-6In 2020 ,《Symmetrical-Tetramethyl-Cucurbit[6]uril-Driven Movement of Cucurbit[7]uril Gives Rise to Heterowheel [4]Pseudorotaxanes》 was published in Journal of Organic Chemistry. The article was written by Lin, Rui-Lian; Li, Ran; Shi, Hao; Zhang, Kun; Meng, Di; Sun, Wen-Qi; Chen, Kai; Liu, Jing-Xin. The article contains the following contents:

Two novel heterowheel [4]pseudorotaxanes consisting of cucurbit[7]uril (Q[7]) and sym.-tetramethyl-cucurbit[6]uril (TMeQ[6]) were constructed via the multirecognition mechanism, in which Q[7] can rotate freely around the horizontal axis, while TMeQ[6] cannot. In the construction process, due to strong repulsive forces between carbonyl portals of two neighboring wheels, the dethreading and movement of the wheels along the axle was observed The dissociation of the [4]pseudorotaxanes was also discussed. The experimental process involved the reaction of 8-Bromooctanoic acid(cas: 17696-11-6Recommanded Product: 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.Recommanded Product: 17696-11-6

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Jiao, Meng-Jie’s team published research in Journal of Organic Chemistry in 2021 | CAS: 1129-28-8

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Quality Control of Methyl 3-(bromomethyl)benzoate Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.

Quality Control of Methyl 3-(bromomethyl)benzoateIn 2021 ,《Visible-Light-Promoted Multistep Tandem Reaction of Vinyl Azides toward the Formation of 1-Tetralones》 was published in Journal of Organic Chemistry. The article was written by Jiao, Meng-Jie; Hu, Qiang; Hu, Xiu-Qin; Xu, Peng-Fei. The article contains the following contents:

A visible-light-driven multistep tandem reaction between vinyl azides 2-R-3-R1-4-R2-C6H2C(=CH2)N3 (R = H, Cl, Me; R1 = H, Me; R2 = H, Br, CN, Ph, etc.) and alkyl bromides R3CH(R4)C((C(O)OCH2CH3)2)Br (R3 = H, prop-1-yn-1-yl, Ph, naphthalen-1-yl, etc.; R4 = H, Me; R3R4 = -(CH2)4-) has been developed leading to the formation of tetralone skeletons I (R5 = H, Me) under mild conditions, which can be easily scaled up to the gram scale. Various 1-tetralone derivatives I are synthesized and transformed into desired products in good to high yields. In the experiment, the researchers used many compounds, for example, Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8Quality Control of Methyl 3-(bromomethyl)benzoate)

Methyl 3-(bromomethyl)benzoate(cas: 1129-28-8) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Quality Control of Methyl 3-(bromomethyl)benzoate Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yang, Qian’s team published research in ACS Applied Materials & Interfaces in 2021 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Recommanded Product: 1,6-Dibromohexane

Yang, Qian; Zhu, Ji-Chun; Li, Zhen-Xing; Chen, Xiao-Shuai; Jiang, Yu-Xing; Luo, Zhi-Wang; Wang, Ping; Xie, He-Lou published an article in 2021. The article was titled 《Luminescent Liquid Crystals Based on Carbonized Polymer Dots and Their Polarized Luminescence Application》, and you may find the article in ACS Applied Materials & Interfaces.Recommanded Product: 1,6-Dibromohexane The information in the text is summarized as follows:

Traditional luminescent liquid crystals (LLCs) suffer from fluorescence quenching caused by aggregation, which greatly limits their further application. In this work, a kind of novel LLCs (named carbonized polymer dot liquid crystals (CPD-LCs)) are designed and successfully synthesized through grafting the rod-shaped liquid crystal (LC) mols. of 4′-cyano-4-(4”-bromohexyloxy) biphenyl on the surface of CPDs. The peripheral LC mols. not only increase the distance between different CPDs to prevent them from aggregating and reduce intermol. energy resonance transfer but also make this LLC have an ordered arrangement. Thus, the obtained CPD-LCs show good LC property and excellent high luminous efficiency with an absolute photoluminescence quantum yield of 14.52% in the aggregated state. Furthermore, this kind of CPD-LC is used to fabricate linearly polarized devices. The resultant linearly polarized dichroic ratio (N) and polarization ratio (ρ) are 2.59 and 0.44, resp. Clearly, this type of CPD-LC shows promising applications for optical devices. In addition to this study using 1,6-Dibromohexane, there are many other studies that have used 1,6-Dibromohexane(cas: 629-03-8Recommanded Product: 1,6-Dibromohexane) was used in this study.

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Recommanded Product: 1,6-Dibromohexane

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Zhang, Chi’s team published research in ACS Applied Materials & Interfaces in 2021 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Recommanded Product: 629-03-8

Zhang, Chi; Fan, Zhinan; Zhan, Hao; Zhou, Hong; Ma, Rongliang; Fan, Li-Juan published an article in 2021. The article was titled 《Fluorescent Cationic Conjugated Polymer-Based Adaptive Developing Strategy for Both Sebaceous and Blood Fingerprints》, and you may find the article in ACS Applied Materials & Interfaces.Recommanded Product: 629-03-8 The information in the text is summarized as follows:

Both latent sebaceous and blood fingerprints may provide valuable information for forensic investigation. To detect both types of fingerprints with no need to predistinguish them, a new adaptive developing strategy was proposed. A cationic conjugated polymer with poly[p-(phenylene ethylene)-alt-(thienylene ethynylene)] backbone (PPETE-NMe3+) was synthesized, which was dissolved in N,N-dimethylformamide (DMF) to form the developing solution Fingerprints were developed by a simple dropping and incubating process without any pre-/post-treatments. Fluorescent photographs of the developed fingerprints on various substrates demonstrated that this developing strategy was effective for both types of fingerprints on nonporous substrates. Gray value anal. further confirmed the enhancement of the legibility of the fingerprint images. The preliminary mechanism exploration suggested that certain weak interactions, such as hydrophobic interaction and electrostatic interaction, may synergistically contribute to the interaction between the polymer and fingerprint components. The mol. design of the polymer combined with an appropriate solvent endowed the developing system the adaptiveness toward different types of fingerprints. This adaptive developing strategy made the fingerprint-developing process more efficient and may be further extended to more practical application scenes.1,6-Dibromohexane(cas: 629-03-8Recommanded Product: 629-03-8) was used in this study.

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Recommanded Product: 629-03-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Narayanan, Sona’s team published research in Materials Today: Proceedings in 2021 | CAS: 3141-27-3

2,5-Dibromothiophene(cas: 3141-27-3) , is mainly used as pharmaceutical intermediate and synthesis intermediate. 2,5-Dibromothiophene may be used as starting reagent for the synthesis of α,α′-didecylquater-, -quinque- and -sexi-thiophenes.Category: bromides-buliding-blocks

Narayanan, Sona; Sreekumar, K.; Joseph, Rani published an article in 2021. The article was titled 《Synthesis and third-order nonlinear optical properties of low band gap 3,4-ethylenedioxythiophene-thiophene copolymers》, and you may find the article in Materials Today: Proceedings.Category: bromides-buliding-blocks The information in the text is summarized as follows:

Alternate donor-acceptor 3,4-ethylenedioxythiophene (EDOT) based copolymers with thiophene and 3-Me thiophene were designed by employing d. functional theory (DFT) in the periodic boundary condition using HSE06 exchange correlation functional and 6-31G basis set. The designed copolymers were synthesized via a simple and facile route, i.e., direct arylation and their third-order nonlinear optical properties were investigated by Z-scan technique. The resultant copolymers, P(EDOT-THP) and P(EDOT-MeTHP) were characterized by spectroscopic anal. The photophys. and electrochem. properties of EDOT-thiophene copolymers were investigated by UV-visible spectra and cyclic voltammetry, resp. The copolymers revealed low band gap and better electronic properties as compared to the homopolymers. The introduction of EDOT unit in the polythiophene leads to decreased HOMO-LUMO energy levels, and the absorption spectra was red shifted when compared with that of the parent compound The nonlinear absorption and nonlinear refraction coefficient of copolymers have been investigated at 532 nm. The optical limiting properties of copolymers have also been measured. The copolymers exhibited strong optical nonlinearity owing to the presence of alternate donor-π-acceptor scheme in the polymers. The results came from multiple reactions, including the reaction of 2,5-Dibromothiophene(cas: 3141-27-3Category: bromides-buliding-blocks)

2,5-Dibromothiophene(cas: 3141-27-3) , is mainly used as pharmaceutical intermediate and synthesis intermediate. 2,5-Dibromothiophene may be used as starting reagent for the synthesis of α,α′-didecylquater-, -quinque- and -sexi-thiophenes.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Jheng, Li-Cheng’s team published research in Polymers (Basel, Switzerland) in 2021 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Computed Properties of C6H12Br2

Jheng, Li-Cheng; Cheng, Cheng-Wei; Ho, Ko-Shan; Hsu, Steve Lien-Chung; Hsu, Chung-Yen; Lin, Bi-Yun; Ho, Tsung-Han published their research in Polymers (Basel, Switzerland) in 2021. The article was titled 《Dimethylimidazolium-Functionalized Polybenzimidazole and Its Organic-Inorganic Hybrid Membranes for Anion Exchange Membrane Fuel Cells》.Computed Properties of C6H12Br2 The article contains the following contents:

A quaternized polybenzimidazole (PBI) membrane was synthesized by grafting a dimethylimidazolium end-capped side chain onto PBI. The organic-inorganic hybrid membrane of the quaternized PBI was prepared via a silane-induced crosslinking process with triethoxysilylpropyl dimethylimidazolium chloride. The chem. structure and membrane morphol. were characterized using NMR, FTIR, TGA, SEM, EDX, AFM, SAXS, and XPS techniques. Compared with the pristine membrane of dimethylimidazolium-functionalized PBI, its hybrid membrane exhibited a lower swelling ratio, higher mech. strength, and better oxidative stability. However, the morphol. of hydrophilic/hydrophobic phase separation, which facilitates the ion transport along hydrophilic channels, only successfully developed in the pristine membrane. As a result, the hydroxide conductivity of the pristine membrane (5.02 x 10-2 S cm-1 at 80°C) was measured higher than that of the hybrid membrane (2.22 x 10-2 S cm-1 at 80°C). The hydroxide conductivity and tensile results suggested that both membranes had good alk. stability in 2M KOH solution at 80°C. Furthermore, the maximum power densities of the pristine and hybrid membranes of dimethylimidazolium-functionalized PBI reached 241 mW cm-2 and 152 mW cm-2 at 60°C, resp. The fuel cell performance result demonstrates that these two membranes are promising as AEMs for fuel cell applications. In the experimental materials used by the author, we found 1,6-Dibromohexane(cas: 629-03-8Computed Properties of C6H12Br2)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Computed Properties of C6H12Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary