181212-91-9 Usage
General Description
(S)-N-Boc-aziridine-2-carboxylic acid is a compound that belongs to the class of aziridine-containing amino acids. It is characterized by a N-tert-butoxycarbonyl (Boc) protecting group on the nitrogen atom of the aziridine ring and a carboxylic acid functional group. (S)-N-Boc-aziridine-2-carboxylic acid has potential applications in organic synthesis, medicinal chemistry, and chemical biology. Its unique structural features make it a valuable building block for the preparation of diverse functionalized molecules, particularly in the context of drug discovery and development. Additionally, its aziridine moiety confers reactivity and selectivity that can be harnessed in the design and synthesis of bioactive compounds and pharmaceutical intermediates. Overall, (S)-N-Boc-aziridine-2-carboxylic acid is a versatile chemical entity with promising applications in various fields of science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 181212-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,2,1 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 181212-91:
(8*1)+(7*8)+(6*1)+(5*2)+(4*1)+(3*2)+(2*9)+(1*1)=109
109 % 10 = 9
So 181212-91-9 is a valid CAS Registry Number.
181212-91-9Relevant articles and documents
Polybasic nitrogen heterocyclic non-natural chiral amino acid and synthesis method thereof
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Paragraph 0063; 0076-0078, (2018/11/22)
The invention relates to a polybasic nitrogen heterocyclic non-natural chiral amino acid and a synthesis method thereof. The amino acid can be applied to molecule building for antibiotic synthesis. According to the synthesis method, 2-aminodiethyl malonate and halogenated alkanes carry out substitution reactions, cyclization reactions, and decarboxylation reactions, and the reaction products are split to obtain the polybasic nitrogen heterocyclic non-natural chiral amino acid. The provided novel synthesis method has the advantages of simple synthesis route, low cost, convenient operation, andeasiness for commercial production, the chiral purity of obtained products is high, and the application prospect is good.
