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Phenoxyacetonitrile

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Phenoxyacetonitrile Basic information
Product Name:Phenoxyacetonitrile
Synonyms:Phenoxyacetonirile;Phenoxyacetonitrile,98%;PHENOXYACETONITRILE;Phenoxymethyl cyanide;Phenoxyacetonitrile 98%;Acetonitrile, 2-phenoxy-;2-PHENOXYACETONITRILE
CAS:3598-14-9
MF:C8H7NO
MW:133.15
EINECS:
Product Categories:Aromatic Nitriles;C8 to C9;Cyanides/Nitriles;Nitrogen Compounds
Mol File:3598-14-9.mol
Phenoxyacetonitrile Structure
Phenoxyacetonitrile Chemical Properties
Boiling point 235-238 °C(lit.)
density 1.09 g/mL at 25 °C(lit.)
refractive index n20/D 1.524(lit.)
Fp >230 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Almost colorless
BRN 2206192
InChI1S/C8H7NO/c9-6-7-10-8-4-2-1-3-5-8/h1-5H,7H2
InChIKeyVLLSCJFPVSQXDM-UHFFFAOYSA-N
SMILESN#CCOc1ccccc1
CAS DataBase Reference3598-14-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22
Safety Statements 36
RIDADR 3276
WGK Germany 3
HazardClass 6.1
PackingGroup III
HS Code 29269090
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
Phenoxyacetonitrile Usage And Synthesis
Chemical Propertiesclear light yellow-brown liquid
UsesPhenoxyacetonitrile is a building block that has been used as a reactant for the preparation of [[(oxo)pyridazinyl]phenoxy]acetonitrile derivatives to be used as vasodilators.
UsesPhenoxyacetonitrile may be used in the synthesis of:
  • 2,4-dihydroxyphenoxyacetophenones
  • methylthio(phenoxy)acetonitrile
  • 2,4-diamino-5-(3,4,5-trimethoxyphenoxy)pyrimidine
References[1] M. HAMANA T. H Y Fujimura. Reactions of quinoline and 4-chloroquinoline 1-oxides with phenoxyacetonitrile, chloromethylphenylsulfone, and methyl-thiomethyl-p-tolylsulfone[J]. Heterocycles, 1987, 25 1: 229-233. DOI:10.3987/S-1987-01-0229.
[2] A. Jonczyk* Essa H M. A SIMPLE PROCEDURE FOR THE PREPARATION OF (METHYL- AND PHENYLTHIO)ARYLOXYACETONITRILES[J]. Organic Preparations and Procedures International, 1993, 25 1: 690-693. DOI:10.1080/00304949309356267.
[3] STOGRYN E L. Synthesis of trimethoprim variations. Replacement of methylene by polar groupings[J]. Journal of Medicinal Chemistry, 1972, 15 2: 200-201. DOI:10.1021/jm00272a019.
Phenoxyacetonitrile Preparation Products And Raw materials
Preparation ProductsCortex aldehyde 50 benzyl alcohol
Tag:Phenoxyacetonitrile(3598-14-9) Related Product Information
2-(2-FORMYL-6-METHOXYPHENOXY)ACETONITRILE 4-(tert-Butyl)phenoxyacetonitrile, tech. 3-(Trifluoromethyl)phenoxyacetonitrile 97%,3-(Trifluoromethyl)phenoxyacetonitrile97%,3-(TRIFLUOROMETHYL)PHENOXYACETONITRILE 3-CHLOROPHENOXYACETONITRILE PHENOXYACETONITRILE 2,3-DIHYDRO-1,4-BENZODIOXINE-2-CARBONITRILE 2-(4-CHLOROPHENOXY)-2-METHYLPROPANENITRILE 2-(4-Chlorophenoxy)acetonitrile (2-Methoxyphenoxy)acetonitrile 2-Chlorophenoxyacetonitrile 2-(2,4-Dichlorophenoxy)acetonitrile 4-Methoxyphenoxyacetonitrile 4-Methylphenoxyacetonitrile 2-(3,5-Dichlorophenoxy)acetonitrile 2-[4-(4,5-Dihydro-1,3-thiazol-2-yl)phenoxy]acetonitrile 2-Bromophenoxyacetonitrile, 99 4-Nitrophenoxyacetonitrile 2-(4-Bromophenoxy)acetonitrile