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Acetamide, 2-cyano-N-ethyl-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

922178-99-2

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922178-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 922178-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,1,7 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 922178-99:
(8*9)+(7*2)+(6*2)+(5*1)+(4*7)+(3*8)+(2*9)+(1*9)=182
182 % 10 = 2
So 922178-99-2 is a valid CAS Registry Number.

922178-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyano-N-ethyl-N-phenylacetamide

1.2 Other means of identification

Product number -
Other names Acetamide,2-cyano-N-ethyl-N-phenyl

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:922178-99-2 SDS

922178-99-2Relevant academic research and scientific papers

One-Pot Synthesis of Quinoxalinones via Tandem Nitrosation/Cyclization of N-Aryl Cyanoacetamides

Wang, Fang,Hu, Bo-Lun,Liu, Lizhi,Tu, Hai-Yong,Zhang, Xing-Guo

, p. 11247 - 11252 (2017)

A new one-pot strategy for the synthesis of quinoxalin-2-ones from the tandem nitrosation/cyclization reaction of N-aryl cyanoacetamides with tert-butyl nitrite has been developed. The dehydrogenative N-incorporation is achieved through a sequence of nitrosation, tautomerization, and cyclization, affording quinoxalin-2-ones in moderate to good yields with good functional group tolerance.

3-Alkylperoxy-3-cyano-oxindoles from 2-Cyano-2-diazo-N-phenyl-acetamides via Cyclizing Carbene Insertion and Subsequent Radical Oxidation

Kischkewitz, Marvin,Daniliuc, Constantin-Gabriel,Studer, Armido

supporting information, p. 1206 - 1209 (2016/03/15)

A transition-metal-free one-pot sequence for the synthesis of 3-peroxy-substituted oxindoles from readily prepared 2-cyano-2-diazo-acetamides is reported. The two-step tandem process includes a highly efficient thermal intramolecular C-H-carbene insertion

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