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AA56514

13797-62-1 | (2-Methyl-thiazol-4-yl)-acetic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $41.00 $29.00 -   +
1g 98% in stock $49.00 $35.00 -   +
5g 98% in stock $178.00 $125.00 -   +
25g 98% in stock $851.00 $596.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA56514
Chemical Name: (2-Methyl-thiazol-4-yl)-acetic acid
CAS Number: 13797-62-1
Molecular Formula: C6H7NO2S
Molecular Weight: 157.1903
MDL Number: MFCD02669593
SMILES: Cc1nc(cs1)CC(=O)O

 

Computed Properties
Complexity: 140  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 2-(2-Methylthiazol-4-yl)acetic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and properties make it a valuable building block in various organic reactions.In chemical synthesis, $name$ serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its thiazole ring provides reactivity and specificity in forming new carbon-carbon and carbon-heteroatom bonds. This makes it particularly useful in the synthesis of complex organic molecules where precise control over functional group connectivity is essential.As a versatile substrate, $name$ can undergo a variety of transformations, including acylation, alkylation, and cross-coupling reactions. Its methylthiazole moiety imparts not only structural diversity but also enhances the biological activity of the final products. This makes $name$ a valuable tool for medicinal chemists in designing and synthesizing new drug candidates with improved potency and selectivity.Moreover, the presence of the carboxylic acid group in $name$ allows for further derivatization through esterification, amidation, or condensation reactions. This enables chemists to tailor the physical and chemical properties of the final compounds for specific applications, ranging from drug delivery systems to functional materials.Overall, the application of 2-(2-Methylthiazol-4-yl)acetic acid in chemical synthesis demonstrates its significance in the field of organic chemistry as a versatile and indispensable building block for designing and accessing diverse molecular structures with desired properties.
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