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4α-[[2-(Acetylamino)-2-deoxy-4-O-sodiosulfo-β-D-glucopyranosyl]oxy]-5β-(hydroxymethyl)-L-proline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95975-85-2

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95975-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95975-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,9,7 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95975-85:
(7*9)+(6*5)+(5*9)+(4*7)+(3*5)+(2*8)+(1*5)=202
202 % 10 = 2
So 95975-85-2 is a valid CAS Registry Number.

95975-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,(2S,4S,5R)-4-[(2R,3R,4R,5S,6R)-3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-sulfooxyoxan-2-yl]oxy-5-(hydroxymethyl)pyrrolidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names F3 monosodium salt

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:95975-85-2 SDS

95975-85-2Upstream product

95975-85-2Downstream Products

95975-85-2Relevant academic research and scientific papers

Electrochemical Oxidation of Proline Derivatives: Total Syntheses of Bulgecinine and Bulgecin C

Barrett, Anthony G. M.,Pilipauskas, Daniel

, p. 2787 - 2800 (2007/10/02)

The influence of structure on the efficiency of the electrochemical C-5 oxidation of (2S,4S)-hydroxyproline carbamate esters is presented.Optimum methoxylation was observed with (2S,4S)-4-acetoxy-1,2-pyrrolidine-dicarboxylic acid 2-methyl 1-(2-(trimethylsilyl)ethyl) ester (19).The corresponding C-5 methoxy derivative 20 was converted into bulgecinine (4) via a stereospecific radical homologation to incorporate the C-5 hydroxymethyl substituent.Bulgecin C (1c) was prepared via a β-stereoselective glycosidation reaction using a 2-azido-2-deoxy-α-D-glucopyranosyl trichloroacetimidate derivative, regiospecific C-4' sulfation, and deprotection.

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