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423564

4-Bromomethyl-3-nitrobenzoic acid

Name: 4-Bromomethyl-3-nitrobenzoic acid
Brand: ALDRICH

97%

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모든 사진(2)

About This Item

Linear Formula:

BrCH₂C₆H₃(NO₂)CO₂H

CAS Number:

55715-03-2

Molecular Weight:

260.04

Beilstein:

1970939

MDL number:

MFCD00216575

UNSPSC 코드:

12352100

PubChem Substance ID:

24866507

NACRES:

NA.22

추천 제품

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Sigma-Aldrich

159549

4-(Bromomethyl)benzoic acid

Sigma-Aldrich

107794

2-Nitrobenzyl bromide

Sigma-Aldrich

S5006

Styrene oxide

Sigma-Aldrich

222518

3-Nitrobenzyl bromide

Sigma-Aldrich

534757

2-(4-Chlorophenyl)oxirane

Sigma-Aldrich

N13054

4-Nitrobenzyl bromide

Sigma-Aldrich

39391

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide

Sigma-Aldrich

130672

N-Hydroxysuccinimide

Sigma-Aldrich

167118

Ethyl 4-bromobutyrate

Sigma-Aldrich

CDS012336

2-(4-formyl-2-methoxy-5-nitrophenoxy)acetic acid

Quality Level

100

분석

97%

양식

solid

mp

127-130 °C (lit.)

solubility

DMF: soluble(lit.)
dichloromethane: soluble(lit.)

작용기

bromo
carboxylic acid
nitro

SMILES string

OC(=O)c1ccc(CBr)c(c1)[N+]([O-])=O

InChI

1S/C8H6BrNO4/c9-4-6-2-1-5(8(11)12)3-7(6)10(13)14/h1-3H,4H2,(H,11,12)

InChI key

QMAHVAFURJBOFV-UHFFFAOYSA-N

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일반 설명

4-Bromomethyl-3-nitrobenzoic acid (BNBA) is a benzoic acid derivative. It has been synthesized by the nitration of 4-bromomethylbenzoic acid using fuming nitric acid. It participates in the synthesis of 3,4-dihydro-2(1H)-quinazolinones and 3,4-dihydro-1H-quinazolin-2-thiones.

애플리케이션

4-Bromomethyl-3-nitrobenzoic acid may be used in the following studies:

As a reactant in the synthesis of 4-bromomethyl-3-nitrobenzoic acid succinimide ester (BNBA-SE).
As a reactant in the synthesis of 4-(2-hydroxyethylmercaptylmethyl)-3-nitrobenzoic acid.
As a reactant in the synthesis of decyl 4-(bromomethyl)-3-nitrobenzoate.
As a reactant in the synthesis of 4-((2-(hydroxymethyl)phenylamino)methyl)-3-nitrobenzoic acid.
As a thiol photo-deprotection reagent.
As a UV-cleavable reagent to functionalize polyacrylamide acryl hydrate (PAAH).
As a photocleavable linker to form localized photoinversion of surface charges inside the colloidal crystal.
As a starting material in the synthesis of 2H-indazole based library using parallel solution-phase methods.
As a reactant in the synthesis of (N-allyloxycarbonyl)-5-aminopent-1-yl 4-bromomethyl-3-nitrobenzoate.