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Phenoxyacetonitrile

Phenoxyacetonitrile ??? ???
?? ??:
3598-14-9
???:
Phenoxyacetonitrile
???(??):
Phenoxyacetonirile;PHENOXYACETONITRILE;Phenoxymethyl cyanide;2-PHENOXYACETONITRILE;Phenoxyacetonitrile,98%;Phenoxyacetonitrile 98%;Acetonitrile, 2-phenoxy-
CBNumber:
CB9287897
???:
C8H7NO
??? ??:
133.15
MOL ??:
3598-14-9.mol

Phenoxyacetonitrile ??

?? ?
235-238 °C(lit.)
??
1.09 g/mL at 25 °C(lit.)
???
n20/D 1.524(lit.)
???
>230 °F
?? ??
2-8°C
??? ??
??? ??
??
?? ?? ?? ??
BRN
2206192
CAS ??????
3598-14-9(CAS DataBase Reference)
??
  • ?? ? ?? ??
??? ?? Xn
?? ???? ?? 20/21/22
????? 36
????(UN No.) 3276
WGK ?? 3
?? ?? 6.1
???? III
HS ?? 29269090
????(GHS): GHS hazard pictograms
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P280 ????/???/???/?????? ?????.
P301+P312 ??? ???? ??? ????(??)? ??? ????.
NFPA 704
1
2 0

Phenoxyacetonitrile C??? ??, ??, ??

??? ??

clear light yellow-brown liquid

??

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.

?? ??

[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 ?? ?? ? ???

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Phenoxyacetonitrile ?? ??

???( 85)?? ??
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Phenoxyacetonitrile ?? ??:

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