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

25354-54-5

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25354-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25354-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,5 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25354-54:
(7*2)+(6*5)+(5*3)+(4*5)+(3*4)+(2*5)+(1*4)=105
105 % 10 = 5
So 25354-54-5 is a valid CAS Registry Number.

25354-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyanilino)but-2-enenitrile

1.2 Other means of identification

Product number -
Other names 3-p-anisidino-crotononitrile

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:25354-54-5 SDS

25354-54-5Downstream Products

25354-54-5Relevant academic research and scientific papers

One-pot conversion of β-aminocrotononitrile to secondary enaminonitriles including chiral ones - Application to synthesis

Chatterjee,Mishra,Dutta Chowdhury,Mahalanabis, Kumar K.

, p. 1164 - 1170 (2005)

A highly efficient one-pot conversion of β-aminocrotononitrile to secondary enaminonitriles including chiral ones is described. In contrast to β-aminocrotononitrile, some of these N-substituted β-enaminonitriles on reacting with acid chlorides show a unique preference for C-terminal selection allowing preparation of pyrazoles without separation of regioisomers. In addition, use of secondary enaminonitriles also provided access to pyrazoles that are not obtainable with primary enaminonitriles owing to an exclusive preference for N-terminal selection.

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