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72578-86-0

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72578-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72578-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,7 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 72578-86:
(7*7)+(6*2)+(5*5)+(4*7)+(3*8)+(2*8)+(1*6)=160
160 % 10 = 0
So 72578-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NOSi/c1-9-6-5-7(8(9)10)11(2,3)4/h7H,5-6H2,1-4H3

72578-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-trimethylsilylpyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names 1-Methyl-3-(trimethylsilyl)-2-pyrrolidinone

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:72578-86-0 SDS

72578-86-0Relevant articles and documents

Synthesis of quaternary α-perfluoroalkyl lactams via electrophilic perfluoroalkylation

Katayev,Václavík,Brüning,Commare,Togni

supporting information, p. 4049 - 4052 (2016/03/15)

Efficient protocols enabling the rapid installation of trifluoromethyl, as well as further functionalized fluoroalkyl groups by an electrophilic perfluoroalkylation of lactam-derived ketene silyl amides (KSAs) using hypervalent iodine reagents 1 and 2 have been developed.

SYNTHESIS AND PROPERTIES OF α-SILYLATED 2-PYRROLIDONE DERIVATIVES

Kramarova, E. P.,Anisomova, N. A.,Baukov, Yu. I.

, p. 1284 - 1290 (2007/10/02)

A method has been described for the synthesis of previously unreported α-silylated N-substituted 2-pyrrolidone derivatives and a study was carried out on the reactions of these compounds with lithium aluminium hydride and electrophilic reagents.

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