Saltar al contenido
Merck
Todas las fotos(2)

Key Documents

View All Documentation

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

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(2)

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

Quality Level

100

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.)

functional group

bromo

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

¿Está buscando productos similares? Visita Guía de comparación de productos

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

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
MKCP6777
MKCN3242
MKCK6864
MKCD2179
MKBZ3483V

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

Busque por un COA

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Cobb JM, et al.
Tetrahedron Letters, 40(5), 1045-1048 (1999)
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
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.
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

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico