156630-85-2 Usage
Molecular structure
A complex chemical compound with a 2-methylmalonic acid core, various functional groups, and substituents.
Tert-butyldimethylsilyl group
A silicon-containing group that contributes to the compound's reactivity and properties.
Oxoazetidin-2-yl moiety
A nitrogen-containing ring structure that may be involved in chemical reactions and synthetic transformations.
(R)-1-(tert-butyldimethylsilyloxy)ethyl side chain
A side chain with a specific stereochemistry that can influence the compound's biological activity and interactions with other molecules.
Unique reactivity
Due to the presence of specific functional groups, the compound may exhibit unique reactivity in chemical reactions.
Potential applications
The compound's unique properties may make it useful in pharmaceutical or synthetic chemistry applications.
Malonic acid component
The presence of a malonic acid group suggests the potential for the compound to participate in various chemical reactions and synthetic transformations.
Azetidin-2-yl component
The presence of an azetidin-2-yl group indicates the possibility of the compound being involved in a range of chemical reactions and synthetic transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 156630-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,6,3 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156630-85:
(8*1)+(7*5)+(6*6)+(5*6)+(4*3)+(3*0)+(2*8)+(1*5)=142
142 % 10 = 2
So 156630-85-2 is a valid CAS Registry Number.
156630-85-2Relevant academic research and scientific papers
Choi, Woo-Baeg,Churchill, Hywyn R. O.,Lynch, Joseph E.,Thompson, Andrew S.,Humphrey, Guy R.,Volante,Reider, Paul J.,Shinkai, Ichiro
, p. 2275 - 2278 (1994)
(3S,4S)-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-4-[(R)-1-carboxyethyl ]-2-azatidinone 7a was prepared from (3R,4R)-4-acetoxy-3-[(R)-1-t-butyldimethylsilyloxy)ethyl]-2-azetidinon e 3 via a sequence involving coupling with 2,2,5-trimethyl-1,3-dioxan-4,6-dione-4, N-silylation, solvolysis of the methylmeldrum's acid moiety and a stereoselective acid catalyzed decarboxylation.
