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Merck
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180025

Sigma-Aldrich

3-Bromoaniline

98%

Sinónimos:

(3-Bromophenyl)amine, (m-Bromophenyl)amine, 1-Amino-3-bromobenzene, 3-Amino-1-bromobenzene, 3-Bromobenzenamine, m-Aminobromobenzene, m-Bromoaniline

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About This Item

Fórmula lineal:
BrC6H4NH2
Número de CAS:
591-19-5
Peso molecular:
172.02
Beilstein/REAXYS Number:
742028
EC Number:
209-704-4
MDL number:
MFCD00007757
UNSPSC Code:
12352100
PubChem Substance ID:
24850844
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.625 (lit.)

bp

251 °C (lit.)

mp

15-18 °C (lit.)

density

1.58 g/mL at 25 °C (lit.)

SMILES string

Nc1cccc(Br)c1

InChI

1S/C6H6BrN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2

InChI key

DHYHYLGCQVVLOQ-UHFFFAOYSA-N

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General description

The in vitro nephrotoxic potential of 3-bromoaniline was studied.

Application

3-Bromoaniline was used in the synthesis of amino substituted quinazoline.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

>446.0 °F

flash_point_c

> 230 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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3-(tert-Butyl)aniline AldrichCPR

Sigma-Aldrich

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Cobb JM, et al.
Tetrahedron Letters, 40(5), 1045-1048 (1999)
Xiao-Feng Wu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(40), 12599-12602 (2012-09-05)
(C), its (O)K! An efficient palladium-catalyzed carbonylative synthesis of 2-alkylbenzoxazinones has been developed. By starting from 2-bromoanilines and acid anhydrides, the corresponding products were isolated in good yields.
G O Rankin et al.
Journal of applied toxicology : JAT, 15(2), 139-146 (1995-03-01)
Haloanilines are commonly used as chemical intermediates in the manufacture of a wide range of products. The purpose of this study was to examine the in vivo nephrotoxic and hepatotoxic potentials of the 3-haloanilines. The in vitro effects of the
L A Khawli et al.
International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 19(3), 297-301 (1992-04-01)
Biotinyl-m-[125I]iodoanilide (BIA) was synthesized by coupling biotin to m-[125I]iodoaniline via a mixed anhydride reaction. m-[125I]Iodoaniline was produced from the tin precursor, which was prepared using a palladium catalyzed reaction of hexabutylditin with m-bromoaniline. The radioiodinated BIA derivative is characterized by
Ali Sarafraz Yazdi et al.
Journal of chromatography. A, 1082(2), 136-142 (2005-07-23)
A novel method for the extraction of aromatic amines present in water samples is produced here coupling two-step liquid-phase microextraction with high performance liquid chromatography by using a monolithic column. The hydrophobic porous polypropylene membranes were used as the interface

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