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3-Bromo-2-methylaniline

Names

[ CAS No. ]:
55289-36-6

[ Name ]:
3-Bromo-2-methylaniline

[Synonym ]:
Benzenamine, 3-bromo-2-methyl-
1-bromo-2-methyl-3-aminobenzene
2-bromo-6-aminotoluene
3-bromo-2-methyl-phenylamine
3-brom-2-methylanilin
EINECS 259-568-5
Benzenamine,3-bromo-2-methyl
3-bromo-2-methyl aniline
3-Bromo-o-toluidine
2-Amino-6-bromotoluene
3-Bromo-2-methylaniline
MFCD00051579

Biological Activity

[Description]:

3-Bromo-2-methylaniline is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
257.0±20.0 °C at 760 mmHg

[ Molecular Formula ]:
C7H8BrN

[ Molecular Weight ]:
186.05

[ Flash Point ]:
109.3±21.8 °C

[ Exact Mass ]:
184.984009

[ PSA ]:
26.02000

[ LogP ]:
2.56

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.609

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
2810

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2921430090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2921430090

[ Summary ]:
HS:2921430090 toluidines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Synthesis, Resolution, and Absolute Configuration of Difunctionalized Tröger's Base Derivatives. Kiehne U, et al.

Chemistry 14(14) , 4246-4255, (2008)

Efficient and Complementary Methods Offering Access to Synthetically Valuable 1, 2-Dibromobenzenes. Diemer V, et al.

European J. Org. Chem. 2011(2) , 327-340, (2011)

A practical synthesis of a PI3K inhibitor under noncryogenic conditions via functionalization of a lithium triarylmagnesiate intermediate Tian Q, et al.

Org. Process Res. Dev. 17(1) , 97-107, (2013)


More Articles


Related Compounds