De la Mare, P B D’s team published research in Journal of the Chemical Society in 1957 | 16426-64-5

Journal of the Chemical Society published new progress about Bromination. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Category: bromides-buliding-blocks.

De la Mare, P. B. D.; Harvey, J. T. published the artcile< Kinetics and mechanisms of aromatic halogen substitution. III. Partial rate factors for the acid-catalyzed bromination of tert-butylbenzene by hypobromous acid>, Category: bromides-buliding-blocks, the main research area is .

The products of acid-catalyzed reaction of tert-BuPh (I) with HOBr in 50% aqueous dioxane were determined, by isotopic dilution, as 37.7% o- (II), 7.2%, m- (III), and 53.2% p-BrC6H4Bu-tert (IV), and 1.9% PhBr (V). Negligible side chain substitution accompanied the reaction, the kinetic form of which was -d[BrOH]/dt = k[ArH][BrOH][H+], with k = 435 1.2 mole-2 min.-1 at 25°, 12 times greater than for C6H6. These results showed that, in a comparison of I with PhMe, the p-position was less reactive, and the m-position was about equally reactive. Significant electrophilic displacement of the tert-Bu group by Br occurred during the reaction. The results were discussed with special reference to the hyperconjugative power of alkyl groups, and to the effect of steric hindrance in determining the reactivity of the o-position. Some nitro derivatives of II, III, and IV were described. III b10 95-7°, nD25 1.5335 and II, b14 102°, nD25 1.5410. II heated at 80° with 1.5 equivalents 98% HNO3 in a mixture of 35% volume/volume H2SO4 and AcOH and the product chromatographed in C6H6 on Al2O3 gave 2,5-Br(O2N)C6H3Bu-tert (VI). The position of the NO2 group was proved as follows: VI (7.5 g.) heated 50 hrs. at 160° with 30% HNO3 in 3 sealed tubes gave about 3% 2,5-Br(O2N)C6H4CO2H, m. 181°. Model experiments showed that 2,4-Br(O2N)C6H3Bu-tert was similarly oxidized to 2,4-Br(O2N)C6H4CO2H, m. 166°. III heated at 80° with 2 equivalents HNO3 in H2SO4435AcOH similarly gave 30% 5,2 (?),4-Br(O2N)2C6H2Bu-tert, m. 92° (from C5H12). IV (5 g.) similarly heated 6 hrs. at 80° under the same nitrating conditions gave a small yield of p-BrC6H4NO2, m. 124°. In the study of the kinetics of bromination the following was a typical run: from a mixture of I (0.00564M), 0.0028M HOBr, and 0.0221M HClO4 in 50% dioxane, aliquot parts were removed at intervals for titration. A blank run with I omitted was made side by side with this measurement. The mean value of k was found to be 435 l.2 mole-2 min.-1 Labeled IV was prepared, NH4Br82 being first shaken with the Br used in the reaction. The product had f.p. 15.7°. To a solution of 10 l. HOBr and 0.05M HClO4 in 50% dioxane was added 19.18 g. I, then 2.37 g. labeled IV was added to the mixture, the mixture extracted with Et2O, and the IV crystallized to give by calculation 9.19 g. IV. Similarly it was shown that 0.308 g. II had been produced in the reaction. III was treated as for II. The mixture contained 0.843 g. active bromo-tert-butylbenzenes, to which was added 11.45 g. inactive III, and the mixture counted, showing that 0.0606 g. III was produced in the reaction. To a mixture which should have contained 1.36 g. mixed active bromo-tert-butylbenzenes was added 12.74 g. V; the mixture extracted, the product nitrated for 2-3 hrs. at 80°, and the product recovered and chromatographed showed that the reaction mixture contained 0.0197 g. V. The conclusion that there was greater hindrance to the entry of NO2 than of Br o- to an alkyl group, was confirmed by this investigation. For I the rate ratios were 0.37 and 0.07, resp., and the free energy difference corresponding to these figures was 0.87 kcal./mole. The effects of hyperconjugation in PhMe and I were considered in some detail. The small proportion of V (1.9 mole-%) determined in the products of bromination was considered significant. The absolute rate of displacement of a tert-Bu group from I was faster than that of displacement of a proton from C6H8.

Journal of the Chemical Society published new progress about Bromination. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Category: bromides-buliding-blocks.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Chen, Xiang-Yu’s team published research in CCS Chemistry in 2019 | 3893-18-3

CCS Chemistry published new progress about Cycloaddition reaction catalysts. 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Related Products of 3893-18-3.

Chen, Xiang-Yu; Zhao, Kun; Liu, Qiang; Zhi, Ying; Ward, James; Rissanen, Kari; Enders, Dieter published the artcile< N-heterocyclic carbene-catalyzed 1,6-addition of homoenolate equivalent intermediates: asymmetric synthesis of nonspirocyclic quaternary oxindoles>, Related Products of 3893-18-3, the main research area is nonspirocyclic diarylmethyl isoxazolyl oxindole ester preparation stereoselective; quinone methide cinnamaldehyde isatin isoxazole cycloaddition heterocyclic carbene catalyst.

Although there is a growing interest in developing asym. 1,6-addition reactions of carbon nucleophiles to Michael acceptors, the corresponding 1,6-addition of homoenolates remains an unsolved problem. Currently, the N-heterocyclic carbene (NHC)-catalyzed cycloadditions of homoenolate equivalent intermediates have achieved widespread success. However, considerable limitations still exist for the linear reactions with electron-deficient alkenes, which are limited to 1,4-Michael acceptors. This report presents the first NHC-catalyzed asym. homoenolate addition of enals to 1,6-Michael acceptors. The strategy leads to the challenging nonspirocyclic 3,3-disubstituted oxindoles with two adjacent stereocenters, a quaternary and a trisubstituted one, in good yields and high stereoselectivities with a wide variety of substrates.

CCS Chemistry published new progress about Cycloaddition reaction catalysts. 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Related Products of 3893-18-3.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Toledo-Sherman, Leticia’s team published research in Journal of Medicinal Chemistry in 2019-03-28 | 16426-64-5

Journal of Medicinal Chemistry published new progress about Crystal structure (X-ray structure of 33 bound to the mutant Vps34 construct). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Synthetic Route of 16426-64-5.

Toledo-Sherman, Leticia; Breccia, Perla; Cachope, Roger; Bate, Jennifer R.; Angulo-Herrera, Ivan; Wishart, Grant; Matthews, Kim L.; Martin, Sarah L.; Cox, Helen C.; McAllister, George; Penrose, Stephen D.; Vater, Huw; Esmieu, William; Van de Poel, Amanda; Van de Bospoort, Rhea; Strijbosch, Annelieke; Lamers, Marieke; Leonard, Philip; Jarvis, Rebecca E.; Blackaby, Wesley; Barnes, Karen; Eznarriaga, Maria; Dowler, Simon; Smith, Graham D.; Fischer, David F.; Lazari, Ovadia; Yates, Dawn; Rose, Mark; Jang, Sung-Wook; Munoz-Sanjuan, Ignacio; Dominguez, Celia published the artcile< Optimization of Potent and Selective Ataxia Telangiectasia-Mutated Inhibitors Suitable for a Proof-of-Concept Study in Huntington's Disease Models>, Synthetic Route of 16426-64-5, the main research area is ATM inhibitor Huntington’s disease mHTT PK PD brain penetrant.

Genetic and pharmacol. evidence indicates that the reduction of ataxia telangiectasia-mutated (ATM) kinase activity can ameliorate mutant huntingtin (mHTT) toxicity in cellular and animal models of Huntington’s disease (HD), suggesting that selective inhibition of ATM could provide a novel clin. intervention to treat HD. Here, we describe the development and characterization of ATM inhibitor mols. to enable in vivo proof-of-concept studies in HD animal models. Starting from previously reported ATM inhibitors, we aimed with few modifications to increase brain exposure by decreasing P-glycoprotein liability while maintaining potency and selectivity. Here, we report brain-penetrant ATM inhibitors that have robust pharmacodynamic (PD) effects consistent with ATM kinase inhibition in the mouse brain and an understandable pharmacokinetic/PD (PK/PD) relationship. Compound 17 engages ATM kinase and shows robust dose-dependent inhibition of X-ray irradiation-induced KAP1 phosphorylation in the mouse brain. Furthermore, compound 17 protects against mHTT (Q73)-induced cytotoxicity in a cortical-striatal cell model of HD.

Journal of Medicinal Chemistry published new progress about Crystal structure (X-ray structure of 33 bound to the mutant Vps34 construct). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Synthetic Route of 16426-64-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Li, Mei-Mei’s team published research in RSC Advances in 2022 | 3893-18-3

RSC Advances published new progress about [3+2] Cycloaddition reaction (regioselective). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Category: bromides-buliding-blocks.

Li, Mei-Mei; Huang, Hui; Tian, Wanrong; Pu, Yiru; Zhang, Chaozheng; Yang, Jirui; Ren, Qing; Tao, Feiyan; Deng, Yun; Lu, Jun published the artcile< Construction of multi-substituted pyrazoles via potassium carbonate-mediated [3 + 2] cycloaddition of in-situ generated nitrile imines with cinnamic aldehydes>, Category: bromides-buliding-blocks, the main research area is methanecarbohydrazonoyl chloride cinnamaldehyde potassium carbonate mediator regioselective cycloaddition; phenyl pyrazole preparation.

A highly efficient potassium carbonate-mediated [3 + 2] cycloaddition reaction of hydrazonoyl chlorides with cinnamic aldehydes to furnish multi-substituted pyrazoles under nontoxic and mild conditions was developed. A plausible stepwise cycloaddition reaction mechanism was proposed. This protocol featured broad substrate coverage, good functional group tolerance, wide scalability, and operational simplicity, as well as conveniently constructed pyrazole scaffolds.

RSC Advances published new progress about [3+2] Cycloaddition reaction (regioselective). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Category: bromides-buliding-blocks.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Han, Xiao-Qing’s team published research in ACS Catalysis in 2022-01-07 | 51605-97-1

ACS Catalysis published new progress about Anilines Role: RCT (Reactant), RACT (Reactant or Reagent). 51605-97-1 belongs to class bromides-buliding-blocks, and the molecular formula is C9H12BrN, Recommanded Product: 2-Bromo-4-isopropylaniline.

Han, Xiao-Qing; Wang, Lei; Yang, Ping; Liu, Jing-Yuan; Xu, Wei-Yan; Zheng, Chao; Liang, Ren-Xiao; You, Shu-Li; Zhang, Junliang; Jia, Yi-Xia published the artcile< Enantioselective Dearomative Mizoroki-Heck Reaction of Naphthalenes>, Recommanded Product: 2-Bromo-4-isopropylaniline, the main research area is naphthoylamino bromoarene palladium catalyst enantioselective dearomative Mizoroki Heck reaction; spirooxindole naphthalene preparation; bromobenzoyl naphthylamine palladium catalyst enantioselective dearomative Mizoroki Heck reaction; spiro oxoisoindoline naphthalene preparation.

A palladium-catalyzed intramol. enantioselective Mizoroki-Heck reaction of naphthalenes was developed via dearomative migratory insertion of an endocyclic π-bond of naphthalene, followed by δ-hydride elimination. This reaction relies on the use of chiral sulfonamide phosphine type Xu-Phos ligand, which successfully inhibited the competitive and undesired C-H arylation reaction and efficiently promoted the formation of spirooxindole and spiroisoindolin-1-one products. Synthetic transformations of the product afforded a series of unique heterocyclic compounds with enantiomeric excess (ee) values retained.

ACS Catalysis published new progress about Anilines Role: RCT (Reactant), RACT (Reactant or Reagent). 51605-97-1 belongs to class bromides-buliding-blocks, and the molecular formula is C9H12BrN, Recommanded Product: 2-Bromo-4-isopropylaniline.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Mahmood, Abid’s team published research in European Journal of Medicinal Chemistry in 2022-03-05 | 51605-97-1

European Journal of Medicinal Chemistry published new progress about Adamantanes Role: PAC (Pharmacological Activity), PRP (Properties), RCT (Reactant), SPN (Synthetic Preparation), THU (Therapeutic Use), BIOL (Biological Study), RACT (Reactant or Reagent), PREP (Preparation), USES (Uses). 51605-97-1 belongs to class bromides-buliding-blocks, and the molecular formula is C9H12BrN, Quality Control of 51605-97-1.

Mahmood, Abid; Ali Shah, Syed Jawad; Iqbal, Jamshed published the artcile< Design and synthesis of adamantane-1-carbonyl thiourea derivatives as potent and selective inhibitors of h-P2X4 and h-P2X7 receptors: An Emerging therapeutic tool for treatment of inflammation and neurological disorders>, Quality Control of 51605-97-1, the main research area is adamantanoyl thiourea preparation SAR receptor inhibitor inflammation docking; Ca(2+) flux assay; Carboxamides; Fura-2 AM dye; Molecular docking studies; P2XR antagonists; Purinergic signaling; Thiourea derivatives.

Adamantane ring has been reported to exhibit significant inhibitory potential towards P2X receptors, especially for P2X7R. Uniqueness of adamantan radicals in synthesized compounds RC(O)NHC(S)NHR1 [R = adamantan-1-yl; R1 = 2-bromo-4-isopropylphenyl, quinolin-8-yl, 3-(dimethylamino)propan-1-yl, etc.] introduced different substitutes to improve potency and selectivity for the P2XR subtypes used. Among synthesized derivatives, RC(O)NHC(S)NHR1 [R = adamantan-1-yl; R1 = 2-bromo-4-isopropylphenyl, quinolin-8-yl] were found to be most potent and selective inhibitors for h-P2X4R and h-P2X7R, resp. Compound RC(O)NHC(S)NHR1 [R = adamantan-1-yl; R1 = 2-bromo-4-isopropylphenyl] was found to be highly selective for h-P2X4R with IC50 ± SEM = 0.04 ± 0.01μM, that is 22 times more potent than BX-430, a standard selective inhibitor of h-P2X4R. Compound RC(O)NHC(S)NHR1 [R = adamantan-1-yl; R1 = quinolin-8-yl] has IC50 ± SEM of 0.073 ± 0.04μM, which is comparable with the known antagonists of h-P2X7R. In silico studies were also conducted to find the type of interactions as well as mode of inhibition. Compound RC(O)NHC(S)NHR1 [R = adamantan-1-yl; R1 = 2-bromo-4-isopropylphenyl, quinolin-8-yl] were studied for mode of inhibition of P2XRs and both were found to be neg. allosteric modulators.

European Journal of Medicinal Chemistry published new progress about Adamantanes Role: PAC (Pharmacological Activity), PRP (Properties), RCT (Reactant), SPN (Synthetic Preparation), THU (Therapeutic Use), BIOL (Biological Study), RACT (Reactant or Reagent), PREP (Preparation), USES (Uses). 51605-97-1 belongs to class bromides-buliding-blocks, and the molecular formula is C9H12BrN, Quality Control of 51605-97-1.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Ghosh, Arghya’s team published research in Organic Letters in 2019-11-01 | 3893-18-3

Organic Letters published new progress about Cyclization catalysts, stereoselective ([3 + 3]). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, SDS of cas: 3893-18-3.

Ghosh, Arghya; Barik, Soumen; Biju, Akkattu T. published the artcile< NHC-Catalyzed [3 + 3] Annulation of Thioamides and Modified Enals for the Enantioselective Synthesis of Functionalized Thiazinones>, SDS of cas: 3893-18-3, the main research area is thiazinone preparation enantioselective; thioamide bromoenal thia Michael addition intramol cyclization.

N-Heterocyclic carbene (NHC)-catalyzed [3 + 3] annulation of thioamides with modified enals allowing the enantioselective synthesis of functionalized 1,3-thiazin-4-ones is reported. The NHC generated from the chiral triazolium salt was optimal and the reaction is initiated by the thia-Michael addition to catalytically generated α,β-unsaturated acylazolium intermediates derived from 2-bromoenals, followed by intramol. cyclization. This operationally simple procedure offers a straightforward and rapid access to target compounds in moderate to good yields and enantiomeric ratio values.

Organic Letters published new progress about Cyclization catalysts, stereoselective ([3 + 3]). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, SDS of cas: 3893-18-3.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Li, Xiaowei’s team published research in Tetrahedron Letters in 2020-06-25 | 3893-18-3

Tetrahedron Letters published new progress about Benzothiazoles Role: SPN (Synthetic Preparation), PREP (Preparation). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Application In Synthesis of 3893-18-3.

Li, Xiaowei; Li, Yuxiu; Liu, Ruihua; Wang, Zemin; Li, Xiangqian; Shi, Dayong published the artcile< AcOH-mediated aerobic oxidative synthesis of 2-thioalkylbenzothiazoles via a three-component reaction>, Application In Synthesis of 3893-18-3, the main research area is aminothiophenol propenal thiophenol acetic acid mediator three component reaction; phenylulfanylalkyl benzothiazole regioselective preparation green chem.

An AcOH-mediated three-component reaction of 2-aminothiophenols, α,β-unsaturated aldehydes, and thiophenols to prepare high value-added 2-(thioalkyl)benzothiazoles, e.g., I, was developed. The reaction was conducted under metal-free conditions, where oxygen served as the terminal oxidant. In addition, this strategy was tolerant of different functional groups, providing efficient access to a variety of functionalized benzothiazole derivatives in moderate to good yields. This reaction has complete regioselectivity and provides a powerful method for building complex mols.

Tetrahedron Letters published new progress about Benzothiazoles Role: SPN (Synthetic Preparation), PREP (Preparation). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Application In Synthesis of 3893-18-3.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Petrovich, P I’s team published research in Zhurnal Obshchei Khimii in 1960 | 16426-64-5

Zhurnal Obshchei Khimii published new progress about Nitration. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, HPLC of Formula: 16426-64-5.

Petrovich, P. I. published the artcile< Oxidative nitration of aromatic compounds. IV. Mercury compounds of some p-disubstituted benzenes and their reaction with nitric acid>, HPLC of Formula: 16426-64-5, the main research area is .

Heating 200 g. p-C6H4Cl2, 40 g. Hg(OAc)2, 60 ml. AcOH, and 1 ml. petr. ether 11.5 hrs. at 125° gave 50% acetoxymercuri-p-dichlorobenzene (I) m. 168.5-9.2°, along with bis(2,5-dichlorophenyl)mercury (II), m. 235-7°. The former with NaCl gave the chloromercuri analog, m. 207-7.5°. Similar reaction of 100 g. p-C6H4Cl2 and 20 g. Hg(OAc)2 in AcOH in the presence of petr. ether in 13 hrs. gave a moderate yield of II, which was also formed by heating I in boiling xylene 10 hrs. I heated without solvent at 172° gave p-C6H4Cl2. II heated with HgCl2 in EtOH-C6H6 gave chloromercuri-p-dichlorobenzene. Oxidation of chloromercuri-p-xylene with KMnO4 in aqueous NaOH at 95° gave 85.3% anhydro-2-(hydroxymercuri)terephthalic acid (Whitmore and Isenhour, CA 23, 4943), which with Br-KBr gave bromoterephthalic acid, m. 298-8.7°. Diazotization of 4-nitro-2-aminotoluene and treatment with HgCl2 gave a colorless 2:1 complex of 4-nitro-2-toluenediazonium chloride and HgCl2, which on conventional decomposition gave 38.8% 2-chloromercuri-4-nitrotoluene, m. 231.5-2°, which with powd. Cu in NH4OH gave bis(4-nitro-2-tolyl)mercury, m. 258.2-8.6°, while oxidation of the former with KMnO4 gave 75% anhydro-2-(hydroxymercuri)-4-nitrobenzoic acid (Whitmore and Middleton, CA 16, 2856), which with Br-KBr gave 2-bromo-4-nitrobenzoic acid, m. 167-8°. I added gradually to 58% HNO3 at 75° and stirred 1.2 hrs. (N oxide formation was caused by gradual addition of paraformaldehyde) gave some 2,5-dichloronitrobenzene (III) and a low yield of 3,6-dichloro-2,4-dinitrophenol (IV), m. 146.2-7°. Similar treatment of II also gave the same product in low yield. Heating 36 g. p-C6H4Cl2, 276 ml. 58% HNO3, 36 g. Hg(NO3)2, 1.2 g. NaNO2, and 1 ml. petr. ether 25 hrs. at 80° gave low yields of III and IV. The above reaction mixture heated in a sealed tube 7 hrs. at 140° (petr. ether omitted) gave HgCl2, 2,5-dichloro-1,3-dinitrobenzene, 2,5-dichloro-1,4-dinitrobenzene and, as the principal product, III (yield not stated). Heating anhydro-2-(hydroxymercuri)terephthalic acid with 58% HNO3 and a trace of NaNO2 (as above) 7 hrs. at 80° in a sealed tube gave 30% nitroterephthalic acid, m. 267-8°. Heating 2-chloromercuri-4-nitrotoluene with 58% HNO3 2.5 hrs. at 50° in the presence of NaNO2 gave a little 2-nitroso-4-nitrotoluene and 2,4-(O2N)2C6H3Me.

Zhurnal Obshchei Khimii published new progress about Nitration. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, HPLC of Formula: 16426-64-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Epperson, James R’s team published research in Bioorganic & Medicinal Chemistry in 2004-09-30 | 6942-39-8

Bioorganic & Medicinal Chemistry published new progress about Homo sapiens. 6942-39-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H6BrFO2, Reference of 6942-39-8.

Epperson, James R.; Bruce, Marc A.; Catt, John D.; Deskus, Jeffrey A.; Hodges, Donald B.; Karageorge, George N.; Keavy, Daniel J.; Mahle, Cathy D.; Mattson, Ronald J.; Ortiz, Astrid A.; Parker, Michael F.; Takaki, Katherine S.; Watson, Brett T.; Yevich, Joseph P. published the artcile< Chronobiotic activity of N-[2-(2,7-dimethoxyfluoren-9-yl)ethyl]-propanamide. Synthesis and melatonergic pharmacology of fluoren-9-ylethyl amides>, Reference of 6942-39-8, the main research area is melatonin receptor agonist methoxy fluorenylethyl propanamide preparation chronobiotic; structure activity melatonin receptor methoxy fluorenylethyl propanamide preparation chronobiotic; biol rhythm chronobiotic methoxy fluorenylethyl amide preparation human.

A series of fluoren-9-yl Et amides were synthesized and evaluated for human melatonin MT1 and MT2 receptor binding. N-[2-(2,7-dimethoxy-9H-fluoren-9-yl)ethyl]propanamide (I) was selected and evaluated in functional assays measuring intrinsic activity at the human MT1 and MT2 receptors and demonstrated full agonism at both receptors. The chronobiotic properties of I were demonstrated in both acute and chronic rat models where I produced an acute phase advance of 32 min at 1 mg/kg and chronically entrained free-running rats with a mean ED of 0.23 mg/kg. I is significantly less efficacious than melatonin in constricting human coronary artery.

Bioorganic & Medicinal Chemistry published new progress about Homo sapiens. 6942-39-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H6BrFO2, Reference of 6942-39-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary