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57402-97-8

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57402-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57402-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57402-97:
(7*5)+(6*7)+(5*4)+(4*0)+(3*2)+(2*9)+(1*7)=128
128 % 10 = 8
So 57402-97-8 is a valid CAS Registry Number.

57402-97-8SDS

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 1-phenyl-N-(trimethylsilylmethyl)methanimine

1.2 Other means of identification

Product number -
Other names benzylidene-trimethylsilanylmethyl-amine

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:57402-97-8 SDS

57402-97-8Relevant articles and documents

NK1 ANTAGONIST

-

Page/Page column 94, (2010/02/09)

The invention is to a compound exhibiting neurokinin inhibitory properties, a pharmaceutical composition comprising same and a method of treatment for neurokinin-meditated conditions.Formula (I)

AZOMETHINE YLIDE PRECURSORS: A SIMPLE ROUTE TO N-(TRIMETHYLSILYLMETHYL) IMINES

Letellier, M.,McPhee, D. J.,Griller, D.

, p. 1975 - 1978 (2007/10/02)

A simple synthesis of N-(trimethylsilylmethyl)amine is reported.This compounds was used to prepare N-(trimethylsilylmethyl)amines, useful sources of "nonstabilized" azomethine ylides.

1,3-Dipolar Cycloaddition Leading to N-Acylated Pyrrolidines and 2,5-Dihydropyrroles

Achiwa, Kazuo,Motoyama, Tadashi,Sekiya, Minoru

, p. 3939 - 3945 (2007/10/02)

Dipolar cycloaddition of an intermediary N-acyltrimethylsilylmethyliminium salt formed from N-(benzylidene)trimethylsilylmethylamine and acyl chloride to conjugated alkenes or alkines gave N-acylpyrrolidines or N-acyl-2,5-dihydropyrroles, respectively.The

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