369648-62-4 Usage
Description
(S)-ethyl 3-(4-(2,7-naphthyridin-1-ylaMino)phenyl)-2-(tert-butoxycarbonylaMino)propanoate is a complex chemical compound derived from ethyl, naphthyridine, and tert-butoxycarbonylamine. It is a propanoate derivative with amino and phenyl functional groups, which are essential for its potential pharmacological properties. (S)-ethyl 3-(4-(2,7-naphthyridin-1-ylaMino)phenyl)-2-(tert-butoxycarbonylaMino)propanoate is characterized by its stereochemistry as (S)-configuration, which is crucial for its biological activity and interactions.
Uses
Used in Organic Synthesis:
(S)-ethyl 3-(4-(2,7-naphthyridin-1-ylaMino)phenyl)-2-(tert-butoxycarbonylaMino)propanoate is used as an intermediate in organic synthesis for the development of various chemical compounds. Its unique structure and functional groups make it a valuable building block for creating novel molecules with specific properties and applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (S)-ethyl 3-(4-(2,7-naphthyridin-1-ylaMino)phenyl)-2-(tert-butoxycarbonylaMino)propanoate is used as a key component in the design and synthesis of new pharmaceuticals. Its potential pharmacological properties, such as its ability to interact with biological targets, make it a promising candidate for the development of drugs targeting various diseases and conditions.
Used in Peptide Synthesis:
The tert-butoxycarbonyl (Boc) protecting group present in the compound is commonly utilized in peptide synthesis. It serves to protect the amine group during the synthesis process, preventing unwanted side reactions and ensuring the correct formation of peptide bonds. This protecting group can be selectively removed when needed, allowing for further modification and functionalization of the molecule.
Used in Pharmaceutical Industry:
(S)-ethyl 3-(4-(2,7-naphthyridin-1-ylaMino)phenyl)-2-(tert-butoxycarbonylaMino)propanoate has practical applications in the pharmaceutical industry, where it can be used as a starting material or a building block for the development of new drugs. Its unique structure and functional groups can be exploited to create molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 369648-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,6,4 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 369648-62:
(8*3)+(7*6)+(6*9)+(5*6)+(4*4)+(3*8)+(2*6)+(1*2)=204
204 % 10 = 4
So 369648-62-4 is a valid CAS Registry Number.
369648-62-4Relevant articles and documents
PHENYLALANINE ENAMIDE DERIVATIVES
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Page 16-17, (2008/06/13)
Phenylalanine enamide derivatives of formula (1) are described, wherein R1is a -CH(CH3)2, -(CH2)2CH3; -CH2C(CH3)3, -CH2CH2OH, -CH2CH2OCH3, -CH2CH2OCH2CH2OH, -CH2CH2OCH2CH2OCH3, formula (A) group; and the salts, solvates and N-oxides thereof. Compounds according to the invention are potent and selective inhibitors of α4 integrins. The compounds are of use in modulating cell adhesion and in particular are of use in the prophylaxis and treatment of diseases or disorders including inflammation in which the extravasation of leukocytes plays a role and the invention extends to such a use and to the use of the compounds for the manufacture of a medicament for treating such diseases or disorders.
