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174195-98-3

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174195-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174195-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,1,9 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174195-98:
(8*1)+(7*7)+(6*4)+(5*1)+(4*9)+(3*5)+(2*9)+(1*8)=163
163 % 10 = 3
So 174195-98-3 is a valid CAS Registry Number.

174195-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2S)-pyrrolidin-2-yl]cyclopentan-1-ol

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:174195-98-3 SDS

174195-98-3Downstream Products

174195-98-3Relevant articles and documents

COMPOUNDS, COMPOSITIONS AND METHODS FOR SYNTHESIS

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Paragraph 00950; 00951; 00956; 00957, (2019/01/10)

The present disclosure, among other things, provides technologies for synthesis, including reagents and methods for stereoselective synthesis. In some embodiments, the present disclosure provides compounds useful as chiral auxiliaries. In some embodiments, the present disclosure provides reagents and methods for oligonucleotide synthesis. In some embodiments, the present disclosure provides reagents and methods for chirally controlled preparation of oligonucleotides. In some embodiments, technologies of the present disclosure are particularly useful for constructing challenging internucleotidic linkages, providing high yields and stereoselectivity.

Enantioselective reduction of ketones with borane catalyzed by cyclic β-amino alcohols prepared from proline

Demir, Ayhan S.,Mecitoglu, Idris,Tanyeli, Cihangir,Guelbeyaz, Volkan

, p. 3359 - 3364 (2007/10/03)

New catalysts have been prepared from (S)- and (R)-proline and the asymmetric borane reduction of prochiral ketones using these catalysts has been studied. The secondary alcohols were obtained in 76-95% yield with 57-96% enantiomeric excesses.

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