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3-Morpholinone, 2-cyclohexylidene-4,5-dimethyl-6-phenyl-, (5S,6R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

402913-43-3

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402913-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 402913-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,9,1 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 402913-43:
(8*4)+(7*0)+(6*2)+(5*9)+(4*1)+(3*3)+(2*4)+(1*3)=113
113 % 10 = 3
So 402913-43-3 is a valid CAS Registry Number.

402913-43-3SDS

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 (5S,6R)-2-cyclohexylidene-4,5-dimethyl-6-phenylmorpholin-3-one

1.2 Other means of identification

Product number -
Other names 3-Morpholinone,2-cyclohexylidene-4,5-dimethyl-6-phenyl-,(5S,6R)

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:402913-43-3 SDS

402913-43-3Relevant articles and documents

Enantioselective synthesis of pantolactone analogues from an ephedrine-derived morpholine-dione

Pansare, Sunil V.,Bhattacharyya, Annyt

, p. 3275 - 3282 (2007/10/03)

An efficient enantioselective synthesis of β,β-dialkyl α-hydroxy γ-butyrolactones, analogues of pantolactone, has been developed employing a stereoselective Prins reaction of chiral alkylidene morpholinones, as the key step. Enantioselective synthesis of a naturally occurring pantolactone homologue and a spiro analogue of pantolactone was achieved with this protocol.

Enantioselective synthesis of β,β-dialkyl α-hydroxy γ-butyrolactones

Pansare, Sunil V.,Bhattacharyya, Annyt

, p. 9265 - 9267 (2007/10/03)

An ephedrine-derived morpholine dione is employed in the synthesis of chiral alkylidene morpholinones that are efficiently converted to β-substituted α,γ-dihydroxy butyramides, precursors of the corresponding butyrolactones. Enantioselective synthesis of a spiro analog of pantolactone as well as a naturally occurring pantolactone homolog is achieved with this protocol.

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