2,6-Difluorobenzyl bromide
Names
[ CAS No. ]:
85118-00-9
[ Name ]:
2,6-Difluorobenzyl bromide
[Synonym ]:
2-(Bromomethyl)-1,3-difluorobenzene
MFCD00000329
FR CF B1E
2,6-Difluorobenzyl bromide
EINECS 285-652-6
α-Bromo-2,6-difluorotoluene
Benzene, 2-(bromomethyl)-1,3-difluoro-
Chemical & Physical Properties
[ Density]:
1.6±0.1 g/cm3
[ Boiling Point ]:
184.9±25.0 °C at 760 mmHg
[ Melting Point ]:
52-55 °C(lit.)
[ Molecular Formula ]:
C7H5BrF2
[ Molecular Weight ]:
207.015
[ Flash Point ]:
65.6±23.2 °C
[ Exact Mass ]:
205.954269
[ LogP ]:
3.06
[ Vapour Pressure ]:
1.0±0.3 mmHg at 25°C
[ Index of Refraction ]:
1.523
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
[ Hazard Codes ]:
C:Corrosive;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S36/37/39-S45-S25
[ RIDADR ]:
UN 3261 8/PG 2
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
8
[ HS Code ]:
2903999090
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. Lett. 16(20) , 5345-9, (2006)
A novel class of inhibitors of pestiviruses (5-substituted 2-phenyl-5H-imidazo[4,5-c]pyridines) is described. Modification of the substituent in position 5 resulted in analogues with high activity (EC...
A convenient one-pot synthesis of asymmetric 1,3,5-triazine-2,4,6-triones and its application towards a novel class of gonadotropin-releasing hormone receptor antagonists.Bioorg. Med. Chem. Lett. 15(3) , 693-8, (2005)
A convenient one-pot synthetic route was developed for the preparation of asymmetric 1,3-dialkyl-1,3,5-triazine-2,4,6-triones from readily available alkyl- or aryl-isocyanates, primary amines and N-ch...
Efficient solid-phase synthesis of quinazoline-2-thioxo-4-ones with SynPhase™ lanterns. Makino S, et al.Tetrahedron Lett. 41(43) , 8333-37, (2000)