3,5-Difluorobenzyl bromide

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Names

[ CAS No. ]:
141776-91-2

[ Name ]:
3,5-Difluorobenzyl bromide

[Synonym ]:
Benzene, 1-(bromomethyl)-3,5-difluoro-
MFCD00010304
alpha-Bromo-3,5-difluorotoluene
α-Bromo-3,5-difluorotoluene
1-(Bromomethyl)-3,5-difluorobenzene
FR CF E1E
3,5-Difluorobenzyl bromide
3,5-Difluoro benzyl bromide

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
205.1±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C7H5BrF2

[ Molecular Weight ]:
207.015

[ Flash Point ]:
81.7±0.0 °C

[ Exact Mass ]:
205.954269

[ LogP ]:
3.06

[ Vapour Pressure ]:
0.4±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 ]:
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 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2903999090

Synthetic Route

Precursor & DownStream

Precursor

  • 3,5-Difluorobenzyl alcohol

DownStream

  • 3,5-Difluorophenylalanine
  • 3,5-Difluorophenylalanine
  • N-ACETYL-3-(3,5-DIFLUOROPHENYL)-DL-ALANINE
  • N-ACETYL-3,5-DIFLUORO-D-PHENYLALANINE
  • Boc-L-3,5-difluorophenylalanine
  • 4-(3,5-DIFLUOROPHENYL)-1-BUTENE
  • 3,5-Difluorotoluene

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

Highly efficient N-heterocyclic carbene/pyridine-based ruthenium sensitizers: complexes for dye-sensitized solar cells.

Angew. Chem. Int. Ed. Engl. 49(44) , 8161-4, (2010)

1-[4-(3,5-Difluoro-benz-yloxy)-2-hy-droxy-phen-yl]ethanone.

Acta Crystallogr. Sect. E Struct. Rep. Online 66(9) , o2468-o2468, (2010)

The title compound, C(15)H(12)F(2)O(3), has been obtained by the reaction of 2,4-dihy-droxy-lacetonephenone, potassium carbonate and 3,5-difluoro-benzyl bromide. The hy-droxy group is involved in an i...


More Articles


Related Compounds

  • 4-Ethoxy-3,5-difluorobenzyl bromide
  • 3,5-Difluorobenzyl alcohol
  • (3,5-Difluorobenzyl)hydrazine hydrochloride
  • 3,5-Difluorobenzyl cyanide
  • 2,5-Difluorobenzyl bromide
  • 2,3-Difluorobenzyl bromide
  • 4-(4-Fluoro-2-trifluoromethyl-phenoxymethyl)-piperidine
  • tert-Butyl (7-(benzylamino)heptyl)carbamate
  • tert-Butyl (7-(cyclobutylamino)heptyl)carbamate
  • 9-((tert-Butyldimethylsilyl)oxy)nonyl 4-methylbenzenesulfonate
  • 3-[4-Chloro-3-(trifluoromethyl)phenoxy]azetidine
  • 3-[4-Chloro-3-(trifluoromethyl)phenoxy]pyrrolidine
  • 2-[5-(Difluoromethyl)-4-iodo-3-methylpyrazol-1-yl]propanoic acid
  • 4-((tert-Butyldimethylsilyl)oxy)-2,2,3,3-tetrafluorobutan-1-ol
  • 4-(6-Fluoro-pyridin-2-yloxy)-piperidine-1-carboxylic acid tert-butyl ester
  • 3-(6-Fluoro-pyridin-2-yloxy)-azetidine-1-carboxylic acid tert-butyl ester
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