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78196-35-7

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78196-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78196-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78196-35:
(7*7)+(6*8)+(5*1)+(4*9)+(3*6)+(2*3)+(1*5)=167
167 % 10 = 7
So 78196-35-7 is a valid CAS Registry Number.

78196-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-glycidyl methacrylate

1.2 Other means of identification

Product number -
Other names -

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:78196-35-7 SDS

78196-35-7Relevant articles and documents

Enantiopure poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate): A new material for supported catalytic asymmetric hydrogen transfer reduction

Rolland, Alice,Herault, Damien,Touchard, Francois,Saluzzo, Christine,Duval, Raphael,Lemaire, Marc

, p. 811 - 815 (2001)

A novel copolymer containing chiral epoxy residues was prepared. Free radical initiated suspension copolymerization of (R)- or (S)-glycidyl methacrylate with ethylene glycol dimethacrylate afforded crosslinked copolymer 1 in high yield. Optically active polymers containing amino alcohol functionalities were then formed from 1 through epoxide ring opening with a number of achiral and homochiral amines. It was shown that ruthenium complexes based on these new polymeric amino alcohol ligands were effective catalysts for the asymmetric hydrogen transfer reduction of acetophenone.

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