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40197-20-4

40197-20-4 Structure

40197-20-4 Structure
IdentificationBack Directory
[Name]

5-BROMO-1H-BENZOIMIDAZOLE-2-CARBOXYLIC ACID
[CAS]

40197-20-4
[Synonyms]

5-Bromo-2-carboxy-1H-benzi
5-Bromo-2-carboxy-1H-benzimidazole
6-Bromo-1H-benzimidazole-2-carboxylic acid
5-BROMO-1H-BENZIMIDAZOLE-2-CARBOXYLIC ACID
5-BROMO-1H-BENZOIMIDAZOLE-2-CARBOXYLIC ACID
1H-Benzimidazole-2-carboxylicacid, 6-bromo-
6-Bromo-1H-benzoimidazole-2-carboxylic acid
5-broMo-1H-1,3-benzodiazole-2-carboxylic acid
5-bromo-1H-benzo[d]imidazole-2-carboxylic acid
6-bromo-1H-benzo[d]imidazole-2-carboxylic acid
5-Bromobenzimidazole-2-carboxylic acid monohydrate
[Molecular Formula]

C8H5BrN2O2
[MDL Number]

MFCD06738769
[MOL File]

40197-20-4.mol
[Molecular Weight]

241.04
Chemical PropertiesBack Directory
[Melting point ]

206℃
[Boiling point ]

495℃
[density ]

1.946
[Fp ]

253℃
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[form ]

powder
[pka]

1.30±0.30(Predicted)
[color ]

Yellow
[InChI]

InChI=1S/C8H5BrN2O2/c9-4-1-2-5-6(3-4)11-7(10-5)8(12)13/h1-3H,(H,10,11)(H,12,13)
[InChIKey]

ULTDLMITPWHISY-UHFFFAOYSA-N
[SMILES]

C1(C(O)=O)NC2=CC(Br)=CC=C2N=1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

5-Bromo-1H-Benzo[d]Imidazole-2-Carboxylic Acid(40197-20-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-(HYDROXYMETHYL)-5-BROMO-1H-BENZOIMIDAZOLE

540516-28-7

5-Bromo-1H-Benzo[d]Imidazole-2-Carboxylic Acid

40197-20-4

General procedure for the synthesis of 5-bromobenzimidazole-2-carboxylic acid from 2-(hydroxymethyl)-5-bromobenzimidazole: 5-bromo-1H-benzimidazol-2-ylmethanol (0.23 g, 1.0 mmol) was dissolved in acetone (10 mL), and an aqueous solution of potassium permanganate (0.379 g, 2.4 mmol) was added (10 mL). After completion of the reaction, the crude product was recrystallized from water to give 5-bromo-1H-benzimidazole-2-carboxylic acid as a creamy white powder in 37% yield.

[References]

[1] Molecules, 2015, vol. 20, # 8, p. 15206 - 15223
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