623564-36-3 Usage
Description
8H-Imidazo[2,1-c][1,4]thiazine-3-carboxaldehyde,5,6-dihydro-(9CI) is a heterocyclic chemical compound that belongs to the imidazo-thiazine family. It features an imidazole ring fused to a thiazine ring, with a carboxaldehyde group at position 3 and 5,6-dihydro substitution. This unique structure and functional groups endow it with potential biological activity, making it a promising candidate for pharmaceutical and medicinal chemistry applications.
Uses
Used in Pharmaceutical Industry:
8H-Imidazo[2,1-c][1,4]thiazine-3-carboxaldehyde,5,6-dihydro-(9CI) is used as a pharmaceutical intermediate for the synthesis of various drug candidates. Its unique structure and functional groups allow for the development of new compounds with potential therapeutic effects.
Used in Medicinal Chemistry Research:
8H-Imidazo[2,1-c][1,4]thiazine-3-carboxaldehyde,5,6-dihydro-(9CI) serves as a key building block in the design and synthesis of novel bioactive molecules. Researchers and scientists can utilize its properties to explore its potential in drug development, targeting various diseases and conditions.
Used in Drug Discovery:
8H-Imidazo[2,1-c][1,4]thiazine-3-carboxaldehyde,5,6-dihydro-(9CI) is employed as a starting material in drug discovery processes. Its unique structure and functional groups can be further modified and optimized to develop new drugs with improved efficacy, selectivity, and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 623564-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,5,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 623564-36:
(8*6)+(7*2)+(6*3)+(5*5)+(4*6)+(3*4)+(2*3)+(1*6)=153
153 % 10 = 3
So 623564-36-3 is a valid CAS Registry Number.
623564-36-3Relevant articles and documents
Bicyclic 6-alkylidene-penems as class-D beta-lactamases inhibitors
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Page/Page column 16, (2010/11/25)
This invention relates to certain bicyclic 6-alkylidene penems which act as a inhibitor of class-D enzymes. β-Lactamases hydrolyze β-lactam antibiotics, and as such serve as the primary cause of bacterial resistance. The compounds of the present invention when combined with β-lactam antibiotics will provide an effective treatment against life threatening bacterial infections. In accordance with the present invention there are provided compounds of general formula I or a pharmaceutically acceptable salt or in vivo hydrolyzable ester R5 thereof: wherein: One of A and B denotes hydrogen and the other an optionally substituted fused bicyclic heteroaryl group; and X═O or S.
PROCESS FOR PREPARING 6-ALKYLIDENE PENEM DERIVATIVES
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Page/Page column 78-79, (2010/02/07)
The present invention provides a process of making compounds of Formula (I), which are useful for the treatment of bacterial infection or disease.
