190141-99-2 Usage
General Description
1-Pyrrolidinecarboxylic acid, 3-amino-4-hydroxy-, 1,1-dimethylethyl ester (9CI) is a chemical compound that falls under the category of amino acids. It is a derivative of pyrrolidinecarboxylic acid and is commonly known as N-tert-butoxycarbonyl-3-amino-4-hydroxy-l-proline. 1-Pyrrolidinecarboxylicacid,3-amino-4-hydroxy-,1,1-dimethylethylester(9CI) is often used in the synthesis of peptides and pharmaceuticals due to its ability to serve as a building block for various bioactive molecules. It has also been studied for its potential in drug development and as a pharmaceutical intermediate. Additionally, it exhibits potential anti-cancer and anti-inflammatory properties, making it an area of interest for further research and development in the medical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 190141-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,1,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 190141-99:
(8*1)+(7*9)+(6*0)+(5*1)+(4*4)+(3*1)+(2*9)+(1*9)=122
122 % 10 = 2
So 190141-99-2 is a valid CAS Registry Number.
190141-99-2Relevant articles and documents
Guanidine derivative and application thereof
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Paragraph 0307; 0309-0312, (2020/06/09)
The invention relates to a guanidine derivative serving as a VAP-1 inhibitor and application of the guanidine derivative, and further relates to a pharmaceutical composition containing the compound. The compound or the pharmaceutical composition can be us
FUSED HETEROCYCLIC COMPOUND
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, (2011/07/29)
The present invention relates to a fused heterocyclic compound having the Formula 1, which is useful as a platelet aggregation inhibitor, a method for preparing the same, and a pharmaceutical composition for inhibiting platelet aggregation comprising the same.
HALOALKYL CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS
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Page/Page column 50-51, (2010/02/11)
The application is directed to haloalkyl-substituted compounds of Formula (I), wherein R1, R1a, R2, R3, R4’ and E are as defined in the claims. The compounds are inhibitors of cysteine proteases, in p