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2-BROMO-5-FLUOROANILINE

Names

[ CAS No. ]:
1003-99-2

[ Name ]:
2-BROMO-5-FLUOROANILINE

[Synonym ]:
ZR CF FE
2-bromo-5-fluoro-aniline
2-Bromo-5-fluoro-phenylamine
2-bromo-5-fluorobenzeneamine
2-Bromo-5-fluoroaniline
MFCD00070750
Benzenamine, 2-bromo-5-fluoro-
benzenamine,2-bromo-5-fluoro
2-Bromo-5-fluorobenzenamine
2-BROMO-5-FLUORO-BENZENAMINE

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
228.2±20.0 °C at 760 mmHg

[ Melting Point ]:
43-47 °C(lit.)

[ Molecular Formula ]:
C6H5BrFN

[ Molecular Weight ]:
190.013

[ Flash Point ]:
91.8±21.8 °C

[ Exact Mass ]:
188.958939

[ PSA ]:
26.02000

[ LogP ]:
2.58

[ Vapour Pressure ]:
0.1±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.597

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 ]:
UN2811

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2921420090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2921420090

[ Summary ]:
HS:2921420090 aniline derivatives and their salts VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

The development of the antitumour benzothiazole prodrug, Phortress, as a clinical candidate.

Curr. Med. Chem. 11(8) , 1009-21, (2004)

This review traces the development of a series of potent and selective antitumour benzothiazoles from the discovery of the initial lead compound, 2-(4-amino-3-methylphenyl)benzothiazole (DF 203) in 19...

Synthesis of isotopically labelled [3-14C]-and [3, 3-2H2]-5-fluoro-1, 3-dihydro-1-hydroxy-2, 1-benzoxaborole (AN2690), a new antifungal agent for the potential treatment of onychomycosis. Baker SJ, et al.

J. Labelled Comp. Radiopharm. 50(4) , 245-250, (2007)

Synthesis of novel benzylamine analogues of Anacardic acid as potent antibacterial agents. Dubey PK.

Der Pharma Chemica 3(6) , 500-512, (2011)


More Articles


Related Compounds

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