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871822-43-4

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871822-43-4 Usage

General Description

(3R,4R)-3,4-Difluoropyrrolidin-1-ylethanol is a compound with the molecular formula C5H9F2NO, which is a fluorinated pyrrolidine derivative. It is a chiral compound that exists in two enantiomeric forms, also known as stereoisomers, 3R,4R and 3S,4S. (3R,4R)-3,4-Difluoropyrrolidin-1-ylethanol has potential applications in medicinal chemistry and drug development due to its unique chemical structure and properties. It may be used in the synthesis of pharmaceutical drugs or as a building block for other organic compounds. Additionally, the presence of fluorine atoms in its structure makes it potentially useful in imaging and diagnostic purposes. Further research and studies may reveal additional uses and applications of (3R,4R)-3,4-Difluoropyrrolidin-1-ylethanol.

Check Digit Verification of cas no

The CAS Registry Mumber 871822-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,8,2 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 871822-43:
(8*8)+(7*7)+(6*1)+(5*8)+(4*2)+(3*2)+(2*4)+(1*3)=184
184 % 10 = 4
So 871822-43-4 is a valid CAS Registry Number.

871822-43-4SDS

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 (3R,4R)-3,4-Difluoropyrrolidin-1-ylethanol

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

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More Details:871822-43-4 SDS

871822-43-4Downstream Products

871822-43-4Relevant 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.

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