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(S)-N-(p-toluenesulphonyl)-2-(morpholinomethyl) pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114671-25-9

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114671-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114671-25-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,7 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114671-25:
(8*1)+(7*1)+(6*4)+(5*6)+(4*7)+(3*1)+(2*2)+(1*5)=109
109 % 10 = 9
So 114671-25-9 is a valid CAS Registry Number.

114671-25-9SDS

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 (S)-N-(p-toluenesulphonyl)-2-(morpholinomethyl) pyrrolidine

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:114671-25-9 SDS

114671-25-9Relevant academic research and scientific papers

PREPARATION OF PROLINE DERIVED LITHIUM AMIDE BASES AND THEIR USE IN ENANTIOSELECTIVE DEPROTONATION OF MESO EPOXIDES

Hendrie, Shirley K.,Leonard, John

, p. 3289 - 3294 (2007/10/02)

An alternative method of preparation for a range of proline derived chiral lithium amide bases is described. (S)-2-(Pyrrolidinomethyl) pyrrolidine, prepared by the new route, has been used to deprotonate cis and trans tbutyldimethylisiloxy-3,4-epoxycyclopentane enantioselectively, thus generating chiral cis and trans tbutyldimethylsiloxy-2-cyclopenten-4-ols.The products had higher enantiomeric purity than those produced when the base was prepared by a previously reported method.

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