2-Triflnoromethoxybenzyl cyanide

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Names

[ CAS No. ]:
137218-25-8

[ Name ]:
2-Triflnoromethoxybenzyl cyanide

[Synonym ]:
2-(Trifluoromethoxy)Phenylacetonitrile
MFCD00236326
2-(Trifluoromethoxy)benzyl Cyanide
2-[2-(trifluoromethoxy)phenyl]acetonitrile
2-Triflnoromethoxybenzyl Cyanide

Chemical & Physical Properties

[ Density]:
1.28 g/mL at 25 °C(lit.)

[ Boiling Point ]:
222-223 °C(lit.)

[ Molecular Formula ]:
C9H6F3NO

[ Molecular Weight ]:
201.14500

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
201.04000

[ PSA ]:
33.02000

[ LogP ]:
2.65128

[ Vapour Pressure ]:
0.175mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.449(lit.)

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
T

[ Risk Phrases ]:
R20/21/22;R36/38

[ Safety Phrases ]:
S26-S36/37/39

[ RIDADR ]:
3276

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2926909090

Precursor & DownStream

Precursor

DownStream

  • 2-(Trifluoromethoxy)phenylacetic acid

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Synthesis of Phloroglucinol Monoaryl Ethers Sherwood AM, et al.

Synthesis 44.08 , 1208-1212, (2012)

Selectivity issues in the catalytic multiphase reduction of functionalized halogenated aromatics over Pd/C, Pt/C, and Raney-Ni Evdokimova, Galina, et al.

Appl. Catal. A Gen. 271.1 , 129-136, (2004)

Fused thiophene derivatives as MEK inhibitors Laing VE, et al.

Bioorg. Med. Chem. Lett. 22.1 , 472-475, (2012)


More Articles

Related Compounds

  • 2-butoxybenzyl cyanide
  • 2-ethylbutanoyl cyanide
  • 2-bromobenzoyl cyanide
  • 2-methoxybenzoyl cyanide
  • 2-methylbenzoyl cyanide
  • 2-phenoxymethylbenzoyl cyanide
  • benzyl {[(2Z)-2-(2,6-dichlorobenzylidene)-3-oxo-2,3-dihydro-1-benzofuran-6-yl]oxy}acetate
  • (2h-3,4-Dihydrobenzopyran-5-yl)methanol
  • (Z)-2-(2-ethoxybenzylidene)-6-((3-methylbut-2-en-1-yl)oxy)benzofuran-3(2H)-one
  • N-(2,1,3-benzoxadiazol-4-yl)-5-bromopyridine-3-carboxamide
  • 7-(5-bromo-2-pyridinyl)-8,9-dimethyl-2-(4-pyridinyl)-7H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine
  • 3,3-Dimethylbutyl trifluoromethanesulfonate
  • 2-methyl-2-{1-[3-(morpholin-4-yl)propyl]-1,2-dihydro[1,3,5]triazino[1,2-a]benzimidazol-3(4H)-yl}propan-1-ol
  • N-(4-methyl-3-phenyl-3H-1,5-benzodiazepin-2-yl)-2-(morpholin-4-yl)acetamide
  • 4-(2-chlorobenzyl)-1-(2-methoxyphenyl)-3-methyl-1H-pyrazol-5-ol
  • 5-[(4-pyrimidin-2-ylpiperazin-1-yl)acetyl]-10,11-dihydro-5H-dibenzo[b,f]azepine