171919-76-9 Usage
Uses
Used in Organic Synthesis:
Tert-butyl (S)-2-methyl-3-oxoazetidine-1-carboxylate is used as a building block or intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure and potential reactivity make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
Tert-butyl (S)-2-methyl-3-oxoazetidine-1-carboxylate is used as a chiral building block in the development of enantioselective synthetic routes for the production of chiral pharmaceuticals. Its specific three-dimensional shape and properties, due to the S stereochemistry, can be utilized to create chiral centers in drug molecules, leading to improved selectivity and potency.
Used in Materials Science:
Tert-butyl (S)-2-methyl-3-oxoazetidine-1-carboxylate may be used as a monomer or precursor in the synthesis of novel materials with unique properties. Its potential reactivity and structural features can be exploited to create new polymers, coatings, or other materials with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 171919-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,9,1 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 171919-76:
(8*1)+(7*7)+(6*1)+(5*9)+(4*1)+(3*9)+(2*7)+(1*6)=159
159 % 10 = 9
So 171919-76-9 is a valid CAS Registry Number.
171919-76-9Relevant academic research and scientific papers
Synthesis of enantiopure dehydropiperidinones from α-amino acids and alkynes via azetidin-3-ones
Ishida, Naoki,Yuhki, Tatsuya,Murakami, Masahiro
scheme or table, p. 3898 - 3901 (2012/09/22)
Chiral dehydropiperidinones were synthesized in enantiopure form from α-amino acids and alkynes via azetidin-3-ones.
Azetidin-3-ones from (S)-α-amino acids and their reactions with nucleophiles: Preparation of some azetidine-containing amino-alcohol and amino-acid derivatives
Podlech,Seebach
, p. 1238 - 1246 (2007/10/02)
The reactions of azetidin-3-ones 6-10, readily available from the amino acids L-alanine, L-phenylalanine, L-valine, L-lysine, and L-aspartic acid, via the corresponding diazo ketones, with nucleophilic reagents such as complex hydrides, Grignard compounds
