Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H5BrO2 |
| Molecular Weight | 201.017 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=C(Br)C=C1
InChI
InChIKey=TUXYZHVUPGXXQG-UHFFFAOYSA-N
InChI=1S/C7H5BrO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Preparative chiral liquid chromatography for enantiomeric separation of pheromones. | 2001 Mar |
|
| pi-Facial selectivities of diastereotopic ketones: p-bromobenzoates of 4-hetero-1-decalinols. | 2001 Sep |
|
| Aromatase inhibitory activities of standishinal and the diterpenoids from the bark of Thuja standishii. | 2002 Aug |
|
| Characterization of bacterial consortia capable of degrading 4-chlorobenzoate and 4-bromobenzoate under denitrifying conditions. | 2002 Aug 6 |
|
| Isolation and structure elucidation of Sch 642305, a novel bacterial DNA primase inhibitor produced by Penicillium verrucosum. | 2003 Dec |
|
| Glochidionionosides A-D: megastigmane glucosides from leaves of Glochidion zeylanicum (Gaertn.) A. Juss. | 2003 Mar |
|
| Isolation and characterization of a lipoxygenase from Pseudomonas 42A2 responsible for the biotransformation of oleic acid into ( S )-( E )-10-hydroxy-8-octadecenoic acid. | 2004 Feb |
|
| Inhibitory effects of 4-halobenzoic acids on the diphenolase and monophenolase activity of mushroom tyrosinase. | 2004 Jul |
|
| Cellular processing in the SW1222 cell line of mAb A33 directly and indirectly radiohalogenated. | 2006 Jul |
|
| NaIO4-mediated selective oxidation of alkylarenes and benzylic bromides/alcohols to carbonyl derivatives using water as solvent. | 2006 Jun 23 |
|
| Toward a magnetostructural correlation for a family of Mn6 SMMs. | 2007 Oct 17 |
|
| Identification of genes coding for hydrolytic dehalogenation in the metagenome derived from a denitrifying 4-chlorobenzoate degrading consortium. | 2008 Apr |
|
| (R)-1-(4-Bromo-benzo-yl)-4-(1-phenyl-prop-yl)thio-semicarbazide. | 2008 Apr 10 |
|
| Diaquabis(4-bromo-benzoato-κO)-bis(N,N'-diethyl-nicotinamide-κN)zinc(II). | 2008 Aug 30 |
|
| Method to determine enantiomeric excess of glucose by nonchiral high-performance liquid chromatography using circular dichroism detection. | 2008 Feb 1 |
|
| Diaqua-bis(4-bromo-benzoato-κO,O')zinc(II). | 2008 Feb 6 |
|
| Layered double hydroxide intercalated with p-methylbenzoate and p-bromobenzoate: molecular simulations and XRD analysis. | 2008 Mar 1 |
|
| Synthesis, anti-bacterial, anti-asthmatic and anti-diabetic activities of novel N-substituted-2-(4-phenylethynyl-phenyl)-1H-benzimidazoles and N-substituted 2[4-(4,4-dimethyl-thiochroman-6-yl-ethynyl)-phenyl)-1H-benzimidazoles. | 2008 May |
|
| Toxicity and quantitative structure-activity relationships of benzoic acids to Pseudokirchneriella subcapitata. | 2009 Jun 15 |
|
| Packing behaviour of two predominant anionic phospholipids of bacterial cytoplasmic membranes. | 2010 Aug |
|
| Preparation and utility of trihaloethyl imidates: useful reagents for the synthesis of amidines. | 2010 Feb 5 |
|
| Bis(4-bromo-benzo-yl)(2,7-dimethoxy-naphthalene-1,8-di-yl)dimethanone. | 2010 Jan 20 |
|
| Tris(1,10-phenanthroline-κN,N')zinc(II) bis-(4-bromo-benzoate) 6.5-hydrate. | 2010 Mar 31 |
|
| (4-Bromo-phen-yl)(3,6-dimeth-oxy-2-naphth-yl)methanone. | 2010 Oct 13 |
|
| Aqua-(4-bromo-benzoato-κO)bis-(1,10-phenanthroline-κN,N')zinc(II) 4-bromo-benzoate 1.5-hydrate. | 2010 Oct 2 |
|
| Tetra-aqua(2,2'-bipyridine-κN,N')magnesium(II) bis-(4-bromo-benzoate). | 2010 Oct 23 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
m2685
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | Merck Index | ||
|
209-581-7
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
17582
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
60698
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
DTXSID7060413
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
176126
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
586-76-5
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
6992P6102O
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
11464
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY | |||
|
143357
Created by
admin on Sat Dec 16 04:19:08 GMT 2023 , Edited by admin on Sat Dec 16 04:19:08 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
