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Propanenitrile, 3-[(2,4-dinitrophenyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15942-22-0

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15942-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15942-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,4 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15942-22:
(7*1)+(6*5)+(5*9)+(4*4)+(3*2)+(2*2)+(1*2)=110
110 % 10 = 0
So 15942-22-0 is a valid CAS Registry Number.

15942-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,4-dinitroanilino)propanenitrile

1.2 Other means of identification

Product number -
Other names N-(2-Cyan-ethyl)-2,4-dinitro-anilin

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:15942-22-0 SDS

15942-22-0Downstream Products

15942-22-0Relevant academic research and scientific papers

Pd(OAc)2-catalyzed dinitration reaction of aromatic amines

Feng, Yi-Si,Mao, Long,Bu, Xiao-Song,Dai, Jian-Jun,Xu, Hua-Jian

, p. 3827 - 3832 (2015/06/02)

Taking advantage of Pd(OAc)2-catalyzed dinitration reactions with Bi(NO3)3·5H2O in trifluoroethanol (TFE) and trifluoroacetic acid (TFA), we have developed an efficient and practical method for the synthesis of secondary dinitro-aromatic amines. The products could be applied to the preparation of 5-amine-N-methyl-benzimidazolone, the azo-dyes, economic advantages. The method has also been expanded to the dinitration reaction of some tertiary aromatic amines.

STRUCTURE AND PROPERTIES OF PYRAZOLINEDIAZONIUM SALTS

Gorelik, M. V.,Titova, S. P.,Rybinov, V. I:

, p. 773 - 781 (2007/10/02)

Study of the IR spectra and reactivity of 1-R-2-pyrazoline-3-diazonium salts indicated the presence of effective electronic interaction between the RN1 group and the diazonium group.In azo coupling and nucleophilic substitution reactions of the

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