Skip to Content
Merck
CN

B56420

2-Bromoaniline

98%

Synonym(s):

2-Amino-1-bromobenzene, 2-Aminobromobenzene, 2-Bromobenzenamine, 2-Bromophenylamine, o-Aminobromobenzene, o-Bromoaniline

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
BrC6H4NH2
CAS Number:
Molecular Weight:
172.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-421-3
Beilstein/REAXYS Number:
742062
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2-Bromoaniline, 98%

InChI key

AOPBDRUWRLBSDB-UHFFFAOYSA-N

InChI

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

SMILES string

Nc1ccccc1Br

assay

98%

form

solid

bp

229 °C (lit.)

mp

24-28 °C (lit.)

density

1.52 g/mL at 25 °C (lit.)

Quality Level

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

2-Bromoaniline is a primary amine that is widely used as a precursor in the synthesis of organobromine compounds.

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

>230.0 °F

flash_point_c

> 110 °C

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Investigating the Effect of Cross-Conjugation Patterns on the Optoelectronic Properties of 7, 7? Isoindigo-Based Materials
Ren S, et al.
Electronics Letters, 12, 3313-3313 (2023)
Jingjing Zhang et al.
Marine drugs, 18(3) (2020-03-20)
Chitosan is an active biopolymer, and the combination of it with other active groups can be a valuable method to improve the potential application of the resultant derivatives in food, cosmetics, packaging materials, and other industries. In this paper, a
Jingjing Zhang et al.
Carbohydrate polymers, 234, 115903-115903 (2020-02-20)
In this study, 2-urea-chitosan oligosaccharide derivatives (2-urea-COS derivatives) and 2,6-diurea-chitosan oligosaccharide derivatives (2,6-diurea-COS derivatives) were successfully designed and synthesized via intermediate 2-methoxyformylated chitosan oligosaccharide. All samples were characterized and compared based on FT-IR, 1H NMR spectroscopy, and elemental analysis. The
Zabiulla et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 95, 419-428 (2017-09-02)
Disrupted redox balance is implicated in multiple pathologies including malignant progression and tumor angiogenesis. In this investigation, we report the design and development of novel and effective ROS detoxifying azo-hydrazone molecules targeting malignant pathologies and neoangiogenesis. A series of azo-derivatives

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service