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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
Structure of 3-BROMOBENZOIC ACID

SMILES

OC(=O)C1=CC=CC(Br)=C1

InChI

InChIKey=VOIZNVUXCQLQHS-UHFFFAOYSA-N
InChI=1S/C7H5BrO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H,9,10)

HIDE SMILES / InChI

Molecular Formula C7H5BrO2
Molecular Weight 201.017
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
In-line coupling of two-phase single drop microextraction and large volume stacking using an electroosmotic flow pump in nonaqueous capillary electrophoresis.
2009-09-11
Toxicity and quantitative structure-activity relationships of benzoic acids to Pseudokirchneriella subcapitata.
2009-06-15
2-(2-Methyl-5-nitro-1H-imidazol-1-yl)ethyl 3-bromo-benzoate.
2009-04-30
3-Bromo-N'-(2-hydroxy-benzyl-idene)benzohydrazide.
2008-01-18
Analysis of the phase solubility diagram of a phenacetin/competitor/beta-cyclodextrin ternary system, involving competitive inclusion complexation.
2001-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:22:50 GMT 2025
Edited
by admin
on Mon Mar 31 19:22:50 GMT 2025
Record UNII
7DCT3A73LX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-BROMOBENZOIC ACID
Systematic Name English
NSC-32739
Preferred Name English
BENZOIC ACID, M-BROMO-
Common Name English
NSC-3980
Code English
BENZOIC ACID, 3-BROMO-
Common Name English
M-BROMOBENZOIC ACID
Systematic Name English
Code System Code Type Description
CHEBI
166850
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY
PUBCHEM
11456
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY
FDA UNII
7DCT3A73LX
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID8060408
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY
CAS
585-76-2
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY
NSC
32739
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-562-3
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY
NSC
3980
Created by admin on Mon Mar 31 19:22:50 GMT 2025 , Edited by admin on Mon Mar 31 19:22:50 GMT 2025
PRIMARY