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Pyrrolidine, 2-[(phenylmethoxy)methyl]-1-[(phenylmethyl)sulfonyl]-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89598-04-9

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89598-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89598-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,9 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89598-04:
(7*8)+(6*9)+(5*5)+(4*9)+(3*8)+(2*0)+(1*4)=199
199 % 10 = 9
So 89598-04-9 is a valid CAS Registry Number.

89598-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-Benzyloxymethyl-1-phenylmethanesulfonyl-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:89598-04-9 SDS

89598-04-9Relevant academic research and scientific papers

Asymmetric Diels-Alder Reactions with Sulfines Derived from Proline

Broek, Leon A. G. M. van den,Porskamp, Pascal A. T. W.,Haltiwanger, R. Curtis,Zwanenburg, Binne

, p. 1691 - 1695 (2007/10/02)

The Synthesis of a variety of sulfines 8 derived from S-proline, utilizing the reaction of α-silyl carbanions with sulfur dioxide, is described.Reaction of the thus prepared sulfines 8 with 2,3-dimethyl-1,3-butadiene gave dihydrothiopyran S-oxides 9.During these cycloaddition reactions asymmetric inductions up to 40percent were observed.From one pure diastereomeric form of cycloadduct 9d an X-ray analysis was carried out in order to provide insight in the steric course of the cycloaddition reaction.

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