4-Bromophenethylamine
Names
[ CAS No. ]:
73918-56-6
[ Name ]:
4-Bromophenethylamine
[Synonym ]:
2-(4-bromophenyl)ethan-1-amine
Benzeneethanamine, 4-bromo-
EINECS 277-636-2
2-(4-Bromophenyl)ethanamine
4-Bromophenethylamine
MFCD00008189
2-(4-Bromophenyl)ethylamine
Biological Activity
[Description]:
[Related Catalog]:
[References]
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
271.3±0.0 °C at 760 mmHg
[ Molecular Formula ]:
C8H10BrN
[ Molecular Weight ]:
200.076
[ Flash Point ]:
113.1±20.4 °C
[ Exact Mass ]:
198.999649
[ PSA ]:
26.02000
[ LogP ]:
2.23
[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C
[ Index of Refraction ]:
1.576
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
C:Corrosive;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S36/37/39-S45
[ RIDADR ]:
UN 2735
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
8.0
[ HS Code ]:
2921499090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2921499090
[ Summary ]:
2921499090 other aromatic monoamines 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
J. Org. Chem. 71 , 5781, (2006)
We have developed two simple and high yielding one-pot syntheses of alkyl aminoaryl sulfides containing a series of four-steps: in situ protection of the free amine by reaction with a Grignard reagent...
Targeted LC-MS derivatization for aldehydes and carboxylic acids with a new derivatization agent 4-APEBA.Anal. Bioanal. Chem 397 , 665-75, (2010)
Based on the template of a recently introduced derivatization reagent for aldehydes, 4-(2-(trimethylammonio)ethoxy)benzeneaminium dibromide (4-APC), a new derivatization agent was designed with additi...
Formation of pyrazinoisoquinoline ring system by the tandem amidoalkylation and N-acyliminium ion cyclization: An efficient synthesis of Praziquantel. Kim JH, et al.Tetrahedron 54(26) , 7395-7400, (1998)