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154132-42-0

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154132-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154132-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,1,3 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 154132-42:
(8*1)+(7*5)+(6*4)+(5*1)+(4*3)+(3*2)+(2*4)+(1*2)=100
100 % 10 = 0
So 154132-42-0 is a valid CAS Registry Number.

154132-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-2-(2-methylsulfanylphenyl)-4-propan-2-yl-4,5-dihydro-1,3-oxazole

1.2 Other means of identification

Product number -
Other names (4S)-4-isopropyl-2-((2-methylthio)phenyl)-1,3-oxazoline

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:154132-42-0 SDS

154132-42-0Downstream Products

154132-42-0Relevant articles and documents

Preparation of Novel Sulfur and Phosphorus Containing Oxazolines as Ligands for Asymmetric Catalysis

Allen, Joanne V.,Dawson, Graham J.,Frost, Christopher G.,Williams, Jonathan M. J.,Coote, Steven J.

, p. 799 - 808 (1994)

The preparation of enantiomerically pure ligands which contain both an oxazoline group and an additional sulfur or phosphorus donor atom are described.Methylthiomethyl, o-thioanisyl and thienyl oxazolines have been prepared in one step, and o-diphenylphosphinophenyl oxazolines have been prepared in two steps in good yields from commercially available starting materials.

Enantioselective palladium catalysed allylic substitution with sulfur-containing oxazoline ligands

Frost,Williams

, p. 1785 - 1788 (2007/10/02)

Enantiomerically pure sulfur/nitrogen ligands have been prepared in one step from amino alcohols and 2-(methylthio)benzonitrile. We have successfully employed these ligands for enantioselective palladium catalysed allylic substitution, with asymmetric ind

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