208338-09-4 Usage
Uses
Used in Pharmaceutical Industry:
(4R,5R)-4,5-BIS(MESYLOXYMETHYL)-1,3,2-DIOXATHIOLANE 2,2-DIOXIDE is used as a key reagent for the synthesis of various pharmaceuticals. Its ability to react with nucleophiles and form different functional groups makes it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (4R,5R)-4,5-BIS(MESYLOXYMETHYL)-1,3,2-DIOXATHIOLANE 2,2-DIOXIDE is employed as a reagent in the production of agrochemicals. Its versatility in forming different functional groups contributes to the creation of effective compounds for agricultural applications.
Used in Organic Synthesis:
(4R,5R)-4,5-BIS(MESYLOXYMETHYL)-1,3,2-DIOXATHIOLANE 2,2-DIOXIDE is used as a versatile reagent in organic synthesis, facilitating the formation of a wide range of functional groups and contributing to the development of various chemical compounds.
Used in Research and Development:
(4R,5R)-4,5-BIS(MESYLOXYMETHYL)-1,3,2-DIOXATHIOLANE 2,2-DIOXIDE is also utilized in research and development for studying its potential pharmacological properties, such as anti-inflammatory and anti-cancer effects, which could lead to the discovery of novel therapeutic agents.
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.
208338-09-4Relevant academic research and scientific papers
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.
