3586-50-3 Usage
General Description
[(methylsulfonyl)oxy]acetic acid, also known as MSAA, is a chemical compound with the molecular formula C3H6O5S. It is a white crystalline solid with a melting point of 140-142°C. MSAA is a derivative of acetic acid and contains a methylsulfonyl group, which contributes to its unique properties. It is commonly used as a raw material or intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. MSAA is also known for its potential as an anti-inflammatory and analgesic agent, making it a subject of interest in the research and development of new drugs. Due to its versatile applications and unique chemical structure, [(methylsulfonyl)oxy]acetic acid is an important compound in the field of organic chemistry and pharmaceutical science.
Check Digit Verification of cas no
The CAS Registry Mumber 3586-50-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3586-50:
(6*3)+(5*5)+(4*8)+(3*6)+(2*5)+(1*0)=103
103 % 10 = 3
So 3586-50-3 is a valid CAS Registry Number.
3586-50-3Relevant articles and documents
Synthesis and radiofluorination of iodophenyl esters as tool for the traceless staudinger ligation
Pretze, Marc,Flemming, Anke,Koeckerling, Martin,Mamata, Constantin
experimental part, p. 1128 - 1136 (2011/01/09)
A new synthetic pathway for the preparation of ω-functionalized 2-iodophenyl esters as starting materials for the synthesis of substituted phosphanes is described. A radiolabeling of these esters with fluorine-18 has led to building blocks which were reacted with HPPh2 in a Pd-catalyzed P-C cross coupling to establish new phosphanes. These compounds can be applied as mild and bioorthogonal radiolabeling agents by means of the traceless Staudinger ligation. A route to access this class of compounds has been established.
Inactivation of liver alcohol dehydrogenases and inhibition of ethanol metabolism by ambivalent active-site-directed reagents
Chen,Bohlken,Plapp
, p. 190 - 193 (2007/10/02)
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