4-Phenoxybenzonitrile

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Names

[ CAS No. ]:
3096-81-9

[ Name ]:
4-Phenoxybenzonitrile

[Synonym ]:
4-Phenoxybenzonitrile
Benzonitrile, 4-phenoxy-
NCR DOR
para-phenoxybenzonitrile
p-phenoxybenzonitrile
4-Phenoxy-benzonitril
4-phenoxybenzenecarbonitrile
4-Cyanodiphenyl Ether
4-phenoxy-benzonitrile
MFCD00017346

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
325.4±25.0 °C at 760 mmHg

[ Melting Point ]:
42-46 °C(lit.)

[ Molecular Formula ]:
C13H9NO

[ Molecular Weight ]:
195.217

[ Flash Point ]:
137.3±17.0 °C

[ Exact Mass ]:
195.068420

[ PSA ]:
33.02000

[ LogP ]:
3.99

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

[ Index of Refraction ]:
1.610

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H332

[ Precautionary Statements ]:
P280

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

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
3439

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2926909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 4-Iodobenzonitrile
  • Phenol
  • 4-Chlorobenzonitrile
  • 4-Nitrobenzonitrile
  • Iodobenzene
  • 4-Hydroxybenzonitrile
  • Trimethyl Phenoxysilane
  • 4-Fluorobenzonitrile
  • Phenylboronic acid
  • Bromobenzene

DownStream

  • 4,4'-Dicyanobiphenyl
  • 4-Hydroxybenzonitrile
  • Benzonitrile
  • Phenol
  • 4-Phenoxybenzylamine
  • 4-Phenoxybenzoic acid
  • 4'-Hydroxy-4-biphenylcarbonitrile
  • 2-(4-Cyanophenyl)phenol
  • 4-Phenoxybenzoic acid methyl ester

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

Microcin C and albomycin analogues with aryl-tetrazole substituents as nucleobase isosters are selective inhibitors of bacterial aminoacyl tRNA synthetases but lack efficient uptake.

ChemBioChem. 13(13) , 1959-69, (2012)

In 1998, Cubist Pharmaceuticals patented a series of aminoacyl tRNA synthetase (aaRS) inhibitors based on aminoacyl sulfamoyladenosines (aaSAs), in which the adenine was substituted by aryl-tetrazole ...

Tris (polyoxaalkyl) amines (trident), a new class of solid-liquid phase-transfer catalysts. Soula G.

J. Org. Chem. 50(20) , 3717-3721, (1985)

CsF/clinoptilolite: an efficient solid base in SNAr and copper-catalyzed Ullmann reactions. Keipour H, et al.

Can. J. Chem. 94(1) , 95-104, (2015)


More Articles

Related Compounds

  • 3-nitro-4-phenoxybenzonitrile
  • 3-Bromo-4-phenoxybenzonitrile
  • 2-chloro-4-phenoxybenzonitrile
  • 2,3,5,6-tetrafluoro-4-phenoxybenzonitrile
  • 4-Bromo-2-phenoxybenzonitrile
  • 4-chlorooxolan-3-ol,formic acid
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
  • N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine