AB46912
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
25g | 97% | in stock | $12.00 | $8.00 | - + | |
100g | 97% | in stock | $16.00 | $11.00 | - + | |
500g | 97% | in stock | $20.00 | $14.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB46912 |
Chemical Name: | Potassium thioacetate |
CAS Number: | 10387-40-3 |
Molecular Formula: | C2H3KOS |
Molecular Weight: | 114.2079 |
MDL Number: | MFCD00137704 |
SMILES: | [S-]C(=O)C.[K+] |
Complexity: | 36.6 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 5 |
Hydrogen Bond Acceptor Count: | 2 |
Potassium thioacetate, also known as potassium mercaptoacetate, is a versatile chemical reagent commonly used in chemical synthesis. It serves as a key building block in the preparation of various sulfur-containing compounds due to its ability to undergo a variety of reactions in organic synthesis.One of the primary applications of potassium thioacetate is in the formation of thioesters, which are important intermediates in organic chemistry. Thioesters are widely used in the synthesis of peptides, pharmaceuticals, and natural products. Potassium thioacetate can react with various organic halides to yield thioester products, making it a valuable tool for chemists working in these areas.Additionally, potassium thioacetate is utilized in the transformation of carbonyl compounds to their corresponding thioacetate derivatives. This reaction, known as the Staudinger reaction, is commonly employed in the modification of functional groups in organic molecules. By using potassium thioacetate, chemists can successfully introduce sulfur-containing moieties in a controlled and efficient manner.Overall, potassium thioacetate plays a crucial role in chemical synthesis by enabling the construction of diverse sulfur-containing compounds with a wide range of applications in pharmaceutical, agricultural, and materials chemistry. Its versatility and reactivity make it an indispensable reagent for synthetic chemists seeking to access novel organic compounds.