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208338-09-4

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208338-09-4 Usage

General Description

The chemical (4R,5R)-4,5-BIS(MESYLOXYMETHYL)-1,3,2-DIOXATHIOLANE 2,2-DIOXIDE is a synthetic compound that contains two mesyloxy (methanesulfonyloxy) groups attached to a 4,5-bis(mesyloxymethyl)-1,3,2-dioxathiolane 2,2-dioxide ring. (4R,5R)-4,5-BIS(MESYLOXYMETHYL)-1,3,2-DIOXATHIOLANE 2,2-DIOXIDE is commonly used as a reagent in organic synthesis and is known for its ability to react with nucleophiles and form a variety of different functional groups. It is often used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, this compound has been studied for its potential pharmacological properties, such as its anti-inflammatory and anti-cancer effects. Overall, (4R,5R)-4,5-BIS(MESYLOXYMETHYL)-1,3,2-DIOXATHIOLANE 2,2-DIOXIDE plays a crucial role in the development of various chemical compounds and has potential applications in the medical and agricultural industries.

Check Digit Verification of cas no

The CAS Registry Mumber 208338-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,3,3 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 208338-09:
(8*2)+(7*0)+(6*8)+(5*3)+(4*3)+(3*8)+(2*0)+(1*9)=124
124 % 10 = 4
So 208338-09-4 is a valid CAS Registry Number.

208338-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4R,5R)-5-(methylsulfonyloxymethyl)-2,2-dioxo-1,3,2-dioxathiolan-4-yl]methyl methanesulfonate

1.2 Other means of identification

Product number -
Other names (4R,5R)-4,5-BIS(MESYLOXYMETHYL)1,3,2-DIOXATHIOLANE 2,2-DIOXIDE

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:208338-09-4 SDS

208338-09-4Downstream Products

208338-09-4Relevant articles and documents

Synthesis of (3S,3S′,4S,4S′)-1,1′-ethylenedipyrrolidine- 3,3′,4,4′-tetraol and related diamino diols: Donor-acceptor hydrogen-bonding motifs of the C2 symmetric 3,4-dihydroxypyrrolidine unit

Marson, Charles M.,Melling, Robert C.,Coles, Simon J.,Hursthouse, Michael B.

, p. 2799 - 2809 (2005)

Enantiopure 1,1′-ethylenedipyrrolidines possessing 3,4-disubstitution have been prepared from esters of l-(+)-tartaric acid. Although diacylation routes via the diacetoxypyrrolidin-2,5-diones were problematic, N,N-dialkylation protocols proved to be reliable and led to the synthesis of (3S,3S′,4S,4S′)-1,1′-ethylenedipyrrolidine-3,3′,4, 4′-tetraol, (3R,3′S,4R,4′S)-3,4-diamino-1,1′- ethylenedipyrrolidine-3′,4′-diol and (3R,3′R,4S,4′S)-3, 3′-diamino-1,1′-ethylenedipyrrolidine-4,4′-diol. The tetraol possesses a crystal structure that exhibits an unusual zig-zag intermolecular pattern comprising a network of hydrogen bonds involving the terminal hydroxyl groups and a nitrogen atom of one of the pyrrolidine rings.

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