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3,4-Pyrrolidinediol, 1-octyl-, (3S,4S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209625-73-0

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209625-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209625-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,6,2 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 209625-73:
(8*2)+(7*0)+(6*9)+(5*6)+(4*2)+(3*5)+(2*7)+(1*3)=140
140 % 10 = 0
So 209625-73-0 is a valid CAS Registry Number.

209625-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4S)-1-n-octylpyrrolidine-3,4-diol

1.2 Other means of identification

Product number -
Other names (3S,4S)-1-Octyl-pyrrolidine-3,4-diol

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:209625-73-0 SDS

209625-73-0Downstream Products

209625-73-0Relevant articles and documents

Enantioselective syntheses of trans-3,4-difluoropyrrolidines and investigation of their applications in catalytic asymmetric synthesis

Marson, Charles M.,Melling, Robert C.

, p. 9771 - 9779 (2007/10/03)

Asymmetric syntheses of enantiopure trans-3,4-difluoropyrrolidines have been prepared by the introduction of fluorine at both centers in a single operation; asymmetric epoxidations and additions to benzaldehyde were conducted using catalysts whose chirality depends on organofluorine asymmetry.

The first enantioselective syntheses of vicinal difluoropyrrolidines and the first catalytic asymmetric synthesis mediated by the C2 symmetry of a -CHFCHF- Unit

Marson, Charles M.,Melling, Robert C.

, p. 1223 - 1224 (2007/10/03)

The first enantiopure vicinal difluorides of C2 symmetry have been prepared by the introduction of fluorine at both centres in a single operation; the first asymmetric synthesis using a catalyst whose chirality depends on organofluorine asymmetry is described.

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