6633-61-0 Usage
Description
Methyl 2-aminothiazole-5-carboxylate, with the CAS number 6633-61-0, is an organic compound that serves as a valuable building block in the synthesis of various complex molecules and pharmaceuticals. Its unique chemical structure, featuring a thiazole ring and a carboxylate group, allows it to participate in a wide range of chemical reactions, making it a versatile component in organic synthesis.
Uses
Used in Pharmaceutical Industry:
Methyl 2-aminothiazole-5-carboxylate is used as an intermediate in the synthesis of various pharmaceutical compounds. Its presence in the molecular structure can contribute to the development of new drugs with potential therapeutic applications, such as antibiotics, anti-inflammatory agents, and other therapeutic molecules.
Used in Organic Synthesis:
Methyl 2-aminothiazole-5-carboxylate is used as a key building block in organic synthesis for the creation of complex organic molecules. Its unique structure allows for a variety of reactions, such as nucleophilic substitution, electrophilic aromatic substitution, and condensation reactions, which can lead to the formation of diverse chemical entities with potential applications in various industries.
Used in Chemical Research:
Methyl 2-aminothiazole-5-carboxylate is used as a research compound in the field of chemistry, particularly in the study of thiazole-containing molecules and their properties. Its reactivity and structural features make it an interesting subject for exploring new reaction pathways, understanding reaction mechanisms, and developing novel synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 6633-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6633-61:
(6*6)+(5*6)+(4*3)+(3*3)+(2*6)+(1*1)=100
100 % 10 = 0
So 6633-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H23NO3/c1-2-26-22(25)20-16-23(21(24)18-11-7-4-8-12-18)14-13-19(20)15-17-9-5-3-6-10-17/h3-12,16,19H,2,13-15H2,1H3
6633-61-0Relevant articles and documents
Thiazolides as novel antiviral agents. 1. Inhibition of hepatitis B virus replication
Stachulski, Andrew V.,Pidathala, Chandrakala,Row, Eleanor C.,Sharma, Raman,Berry, Neil G.,Iqbal, Mazhar,Bentley, Joanne,Allman, Sarah A.,Edwards, Geoffrey,Helm, Alison,Hellier, Jennifer,Korba, Brent E.,Semple, J. Edward,Rossignol, Jean-Francois
scheme or table, p. 4119 - 4132 (2011/08/05)
We report the syntheses and activities of a wide range of thiazolides [viz., 2-hydroxyaroyl-N-(thiazol-2-yl)amides] against hepatitis B virus replication, with QSAR analysis of our results. The prototypical thiazolide, nitazoxanide [2-hydroxybenzoyl-N-(5-
BROADSPECTRUM SUBSTITUTED BENZISOXAZOLE SULFONAMIDE HIV PROTEASE INHIBITORS
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Page/Page column 26, (2008/06/13)
The present invention concerns the compounds having the formula N-oxides, salts, stereoisomeric forms, racemic mixtures, prodrugs esters and metabolites thereof.It further relates to their use as broadspectrum HIV protease inhibitors, processes for their preparation as well as pharmaceutical compositions and diagnostic kits comprising them. It also concerns combinations thereof with another anti-retroviral agent, and to their use in assays as reference compounds or as reagents.
ALPHA- AND BETA-AMINO ACID HYDROXYETHYLAMINO SULFONAMIDES USEFUL AS RETROVIRAL PROTEASE INHIBITORS
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, (2008/06/13)
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