181212-91-9 Usage
Uses
Used in Organic Synthesis:
(S)-N-Boc-aziridine-2-carboxylic acid is used as a key intermediate for the synthesis of complex organic molecules, leveraging its reactivity and selectivity to facilitate the formation of desired products with high efficiency and specificity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-N-Boc-aziridine-2-carboxylic acid is utilized as a building block for the development of novel bioactive compounds. Its unique structural features contribute to the design of pharmaceuticals with improved potency, selectivity, and pharmacokinetic properties.
Used in Chemical Biology:
(S)-N-Boc-aziridine-2-carboxylic acid is employed as a tool compound in chemical biology to probe and modulate biological processes. Its reactivity allows for the selective labeling of biomolecules, enabling researchers to study protein function, enzyme mechanisms, and cellular pathways.
Used in Drug Discovery and Development:
(S)-N-Boc-aziridine-2-carboxylic acid is used as a versatile starting material in the discovery and development of new drugs. Its potential to be incorporated into diverse chemical scaffolds facilitates the exploration of novel therapeutic agents with improved efficacy and safety profiles.
Used in Pharmaceutical Intermediates:
In the pharmaceutical industry, (S)-N-Boc-aziridine-2-carboxylic acid is used as a crucial intermediate in the synthesis of active pharmaceutical ingredients. Its unique structural elements and reactivity contribute to the production of advanced drug candidates with targeted therapeutic effects.
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 academic research and scientific papers
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.
MELANOCORTIN RECEPTOR AGONISTS
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Page/Page column 49, (2010/02/11)
The present invention relates a compound of formula 1, and pharmaceutically acceptable salt, hydrate, solvate, or isomer thereof effective as agonist of melanocortin receptor, and an agonistic composition of melanocortin receptor comprising the same as active ingredient.
