881168-37-2 Usage
Chemical structure
A complex chemical compound consisting of a pyrrolidine moiety, carboxylic acid groups, diphenylsilyl groups, and a propenyl group.
Functional groups
Carboxylic acid groups, diphenylsilyl groups, and a propenyl group.
Substituents
The presence of the 1,1-dimethylethyl group and the ester functionality.
Stereochemistry
The stereochemistry of the compound is specified as 2R,5S.
Potential applications
Likely has potential applications in the pharmaceutical or chemical industries.
Further research
Further research and analysis would be needed to determine its specific uses and properties.
Ester functionality
The presence of the 1,1-dimethylethyl group and the ester functionality adds complexity to the molecule.
Molecular complexity
The molecule is complex due to the presence of multiple functional groups and stereochemistry.
Chirality
The compound has chiral centers at the 2nd and 5th positions, as indicated by the 2R,5S stereochemistry.
Potential reactivity
The compound may have potential reactivity with other molecules due to the presence of carboxylic acid groups and the ester functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 881168-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,1,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 881168-37:
(8*8)+(7*8)+(6*1)+(5*1)+(4*6)+(3*8)+(2*3)+(1*7)=192
192 % 10 = 2
So 881168-37-2 is a valid CAS Registry Number.
881168-37-2Relevant academic research and scientific papers
Stereoselective synthesis of 2,5-di- and 2,2,5-trisubstituted pyrrolidines by allylation reacton of acyliminium ion
Shinada, Tetsuro,Hamada, Makoto,Kawasaki, Masanori,Ohfune, Yasufumi
, p. 511 - 525 (2007/10/03)
-Allylation reactions of allytrimethylsilane and an allylcopper reagent to acyliminium ions derived from several 2-monosubstituted and 2,2-disubstituted pyrrolidinones were examined. These reactions proceeded in a stereoselective manner to give the corresponding allylated adducts. The stereochemical outcomes of these reactions were dependent upon the allylating reagents or the structures of the acyliminium ions.
