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66582-22-7

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66582-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66582-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66582-22:
(7*6)+(6*6)+(5*5)+(4*8)+(3*2)+(2*2)+(1*2)=147
147 % 10 = 7
So 66582-22-7 is a valid CAS Registry Number.

66582-22-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-4-phenyl-butyronitrile

1.2 Other means of identification

Product number -
Other names 3-phenylpropanoyl cyanide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66582-22-7 SDS

66582-22-7Relevant academic research and scientific papers

Synthesis of α,α-difluoronitriles from acyl cyanides

Bartmann, Ekkehard,Krause, Joachim

, p. 117 - 122 (1993)

Aromatic α,α-difluoronitriles (aryl α,α-difluoroacetonitriles) have been synthesized by reaction of aroyl cyanides with diethylamino sulphur trifluoride.Some liquid crystalline difluoronitriles have been prepared by this method.

Trimethylsilyl Cyanide - A Reagent for Umpolung, IX. Enol Esters of Acyl Cyanides: Syntheses and General Properties

Hertenstein, Ulrich,Huenig, Siegfried,Reichelt, Helmut,Schaller, Rainer

, p. 699 - 721 (2007/10/02)

According to Scheme 1 acyl cyanide-enol sulfonates 3-5, carboxylates 7-9, and phosphates 12 are synthesized on routes A-D in generally good yields.Judged by 13C NMR chemical shifts of C-3, the donor effect of the enol groups on the C=C bond decreases slightly in the order OP(O)(OEt)2 > OCO2Et > OCOCH3 > OCOCF3 > OSO2Me OSO2Ph > OSO2C4F9, but being always larger than the acceptor effect of the CN group.Reactions with nucleophiles to give 1,2-diketones (29, 30) and with radicals to form adducts 32 and 35 are described.Depending on the substituent pattern , and cycloadditions can be performed with 2f, 5f, and 12f.Different cyclopropanes 54 can be prepared from 5f.

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