AB55804
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $12.00 | $9.00 | - + | |
1g | 98% | in stock | $23.00 | $17.00 | - + | |
5g | 98% | in stock | $55.00 | $38.00 | - + | |
25g | 98% | in stock | $221.00 | $155.00 | - + | |
100g | 95% | in stock | $853.00 | $597.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB55804 |
Chemical Name: | (S)-(-)-2-Acetoxypropionic acid |
CAS Number: | 6034-46-4 |
Molecular Formula: | C5H8O4 |
Molecular Weight: | 132.1146 |
MDL Number: | MFCD00191370 |
SMILES: | CC(=O)O[C@H](C(=O)O)C |
Complexity: | 129 |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 3 |
XLogP3: | 0.1 |
(S)-2-Acetoxypropanoic acid, also known as (S)-2-hydroxy-1-methylethyl acetate, is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a chiral building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. In chemical synthesis, (S)-2-Acetoxypropanoic acid serves as a valuable precursor for the preparation of chiral intermediates and final products with high stereochemical purity. Its unique stereochemistry allows for the creation of asymmetric carbon centers, which are crucial in the production of complex molecules with specific biological activities. This compound is particularly valued in asymmetric synthesis, where the control of stereochemistry is essential for creating molecules with desired pharmacological or biological properties. By utilizing (S)-2-Acetoxypropanoic acid as a starting material, chemists can access a wide range of enantiomerically pure compounds that are vital in the pharmaceutical industry for the development of new drugs and therapies. Overall, the application of (S)-2-Acetoxypropanoic acid in chemical synthesis enables the efficient and selective construction of chiral molecules, opening up pathways to novel compounds with enhanced biological activities and potential therapeutic benefits.