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2-Pyrrolidinone, 5-(hydroxymethyl)-3,4-bis(phenylmethoxy)-, (3S,4R,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

157831-28-2

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157831-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157831-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,8,3 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 157831-28:
(8*1)+(7*5)+(6*7)+(5*8)+(4*3)+(3*1)+(2*2)+(1*8)=152
152 % 10 = 2
So 157831-28-2 is a valid CAS Registry Number.

157831-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R,5S)-3,4-dibenzyloxy-5-hydroxymethyl-pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names (3S,4R,5S)-3,4-Bis-benzyloxy-5-hydroxymethyl-pyrrolidin-2-one

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:157831-28-2 SDS

157831-28-2Downstream Products

157831-28-2Relevant academic research and scientific papers

Synthetic studies of carzinophilin. Part 2: Synthesis of 3,4-dibenzyloxy-2-methylidene-1-azabicyclo[3.1.0]hexane systems corresponding to the C1-C17 fragment of carzinophilin

Hashimoto, Masaru,Matsumoto, Miyoko,Terashima, Shiro

, p. 3041 - 3062 (2007/10/03)

A model compound bearing the C1-C17 fragment of carzinophilin was synthesized. The synthesis involved coupling reaction of a cyclic thioimidate with the 4H-oxazol-5-one derivative, ring-opening of the 4H-oxazol-5-one to furnish a dehydropeptide system, elaboration of the C1-C6 enolamide, and construction of the aziridine ring as key steps.

A Stereoselective Synthesis of a Novel Model Compound of Carzinophilin Carrying the C6-C13 Unit with Correct Stereochemistry

Nashimoto, Masaru,Terashima, Shiro

, p. 1001 - 1002 (2007/10/02)

The title synthesis was achieved by featuring stereocontrolled elaboration of the functionalized pyrrolidine-2-thione from 2,3,5-tri-O-benzyl-β-D-arabinofuranose and base-induced construction of an aziridine ring from the 5-mesyloxymethylpyrrolidine.

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