4-(Hydroxymethyl)benzonitrile

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Names

[ CAS No. ]:
874-89-5

[ Name ]:
4-(Hydroxymethyl)benzonitrile

[Synonym ]:
MFCD00870633
Benzonitrile, 4-(hydroxymethyl)-
4-(Hydroxymethyl)benzonitrile

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
297.4±23.0 °C at 760 mmHg

[ Melting Point ]:
39-43ºC(lit.)

[ Molecular Formula ]:
C8H7NO

[ Molecular Weight ]:
133.147

[ Flash Point ]:
133.6±22.6 °C

[ Exact Mass ]:
133.052765

[ PSA ]:
44.02000

[ LogP ]:
0.47

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.572

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H315-H319-H332-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
26-36

[ RIDADR ]:
UN 3439

[ WGK Germany ]:
3.0

[ HS Code ]:
2926909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 4-Cyanobenzoic acid
  • 4-Cyanobenzaldehyde
  • 4-Bromobenzyl alcohol
  • Sodium cyanide
  • 4-Cyanobenzylamine
  • tert-Butyl azetidine-3-carboxylate acetate
  • Methyl 4-cyanobenzoate
  • 4-Aminomethylbenzyl alcohol
  • 3-Pyridinecarboxamide,1,4-dihydro-1-(phenylmethyl)-

DownStream

  • (4-Cyanophenyl)acetic acid
  • 4-Cyanobenzoyl chloride
  • 4-Aminomethylbenzyl alcohol
  • 2-(4-CYANOPHENYL)BENZOTHIAZOLE
  • (4-cyanophenyl)methyl acetate
  • 4-cyano-benzoic acid benzyl ester
  • 4-Cyano-N,N-dimethylbenzamide
  • 4-Cyanobenzamide
  • tert-Butyl 4-(bromomethyl)benzylcarbamate
  • 4-(Hydroxymethyl)benzoic 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

Vinyl monomers bearing chromophore moieties and their polymers. VIII. synthesis and fluorescence behavior of a vinyloxy monomer having an electron-accepting chromophore moiety, p-((vinyloxy) methyl) benzonitrile, and its polymers. Du FS, et al.

J. Polym. Sci. A Polym. Chem. 37(2) , 179-187, (1999)

Bu4N [Fe (CO)3(NO)]-Catalyzed Hydrosilylation of Aldehydes and Ketones. Dieskau AP, et al.

European J. Org. Chem. 27 , 5291-5296, (2011)

Bergsträßer U, et al.

Science of Synthesis: Houben-Weyl Methods of Molecular Transformations , (2014), 219


More Articles

Related Compounds

  • 2-bromo-4-(hydroxymethyl)benzonitrile
  • 3-Ethyl-4-(hydroxymethyl)benzonitrile
  • 3-Bromo-4-(hydroxymethyl)benzonitrile
  • 2-chloro-4-(hydroxymethyl)benzonitrile
  • 2-Fluoro-4-(hydroxymethyl)benzonitrile
  • 3-fluoro-4-(hydroxymethyl)benzonitrile
  • 3-(2-bromophenyl)-5-(propan-2-yl)-1H-1,2,4-triazole
  • 5-bromo-3,3-diethyl-2,3-dihydro-1H-indole
  • 3-(Phenylmethanesulfinylmethyl)aniline
  • 1-(5-Bromothiophen-2-yl)-2,2-dimethylpropan-1-amine
  • 5-Methyl-3-sulfanyl-[1,2,4]triazolo[3,4-b][1,3]thiazole-6-carboxylic acid
  • Methyl 4-{[[(4-cyanophenyl)sulfonyl](pyridin-2-ylmethyl)amino]methyl}benzoate
  • N-(4-cyanobenzyl)-4-ethoxy-N-(pyridin-2-ylmethyl)benzenesulfonamide
  • tert-butyl 3-(4-methyl-1H-pyrazol-1-yl)azetidine-1-carboxylate
  • Tert-butyl (6-formyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate
  • 2-(4-Chloro-3-methoxyphenyl)acetaldehyde
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