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Phenoxyacetonitrile

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Phenoxyacetonitrile Basic information

Product Name:
Phenoxyacetonitrile
Synonyms:
  • Phenoxyacetonirile
  • Phenoxyacetonitrile,98%
  • 2-PHENOXYACETONITRILE
  • PHENOXYACETONITRILE
  • Phenoxymethyl cyanide
  • Phenoxyacetonitrile 98%
  • Acetonitrile, 2-phenoxy-
CAS:
3598-14-9
MF:
C8H7NO
MW:
133.15
Product Categories:
  • Aromatic Nitriles
  • C8 to C9
  • Cyanides/Nitriles
  • Nitrogen Compounds
Mol File:
3598-14-9.mol
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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.)
Flash point:
>230 °F
storage temp. 
2-8°C
form 
clear liquid
color 
Colorless to Almost colorless
BRN 
2206192
CAS DataBase Reference
3598-14-9(CAS DataBase Reference)
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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

MSDS

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Phenoxyacetonitrile Usage And Synthesis

Chemical Properties

clear light yellow-brown liquid

Uses

Phenoxyacetonitrile 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.

Uses

Phenoxyacetonitrile 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.

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