1-Bromo-2,4-difluorobenzene
Names
[ CAS No. ]:
348-57-2
[ Name ]:
1-Bromo-2,4-difluorobenzene
[Synonym ]:
2,4-Difluorophenyl bromide
2,4-Difluorobromobenzene
Bromo-2,4-difluorobenzene
1-Bromo-2,4-difluoro
1-bromo-2,4-difluoro-benzene
2,4-diFC6H3Br
Benzene,1-bromo-2,4-difluoro
EINECS 206-479-4
Benzene, 1-bromo-2,4-difluoro-
2,4-Difluoro-1-bromobenzene
1-Bromo-2,4-difluorobenzene
4-Bromo-1,3-difluorobenzene
FR CF DE
2,4-Difluoro
MFCD00000330
Chemical & Physical Properties
[ Density]:
1.7±0.1 g/cm3
[ Boiling Point ]:
148.4±20.0 °C at 760 mmHg
[ Melting Point ]:
−4 °C(lit.)
[ Molecular Formula ]:
C6H3BrF2
[ Molecular Weight ]:
192.989
[ Flash Point ]:
51.7±0.0 °C
[ Exact Mass ]:
191.938614
[ LogP ]:
2.98
[ Vapour Pressure ]:
5.4±0.3 mmHg at 25°C
[ Index of Refraction ]:
1.507
[ Storage condition ]:
2-8°C
[ Water Solubility ]:
INSOLUBLE
MSDS
Safety Information
[ Symbol ]:
GHS02, GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H226-H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
Xi:Irritant
[ Risk Phrases ]:
R10;R36/37/38
[ Safety Phrases ]:
S16-S26-S36/37/39-S37/39
[ RIDADR ]:
UN 1993 3/PG 3
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
3
[ HS Code ]:
29036990
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2903999090
[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
Articles
Bioorg. Med. Chem. 12(9) , 2225-38, (2004)
A series of (2R,3S)-2-(2,4-difluorophenyl)-3-(5-[2-[4-aryl-piperazin-1-yl]-ethyl]-tetrazol-2-yl)-1-[1,2,4]-triazol-1-yl-butan-2-ol (11a-n) and (2R,3S)-2-(2,4-difluorophenyl)-3-(5-[2-[4-aryl-piperazin-...
Regioselective ortho-lithiation of chloro and bromo substituted fluoroarenes. Mongin F and Schlosser M.Tetrahedron Lett. 37(36) , 6551-54, (1996)
A practical chemoenzymatic synthesis of a key intermediate of antifungal agents. Yasohara Y, et al.
Tetrahedron Lett. 42(19) , 3331-3, (2001)