AB47723
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $232.00 | $162.00 | - + | |
250mg | 97% | in stock | $325.00 | $228.00 | - + | |
1g | 97% | in stock | $791.00 | $554.00 | - + | |
5g | 97% | in stock | $2,811.00 | $1,968.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB47723 |
Chemical Name: | 1-Propanone, 3-hydroxy-1-phenyl- |
CAS Number: | 5650-41-9 |
Molecular Formula: | C9H10O2 |
Molecular Weight: | 150.1745 |
MDL Number: | MFCD00135861 |
SMILES: | OCCC(=O)c1ccccc1 |
Complexity: | 126 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 3 |
XLogP3: | 1 |
1-Propanone, 3-hydroxy-1-phenyl- is a key intermediate in chemical synthesis, particularly in organic chemistry. This versatile compound plays a crucial role in various synthetic pathways, serving as a building block for the creation of more complex molecules. Its unique structure, characterized by the presence of both a ketone and a hydroxy group, enables it to participate in a wide range of chemical reactions.In chemical synthesis, 1-Propanone, 3-hydroxy-1-phenyl- is often used as a precursor for the synthesis of pharmaceutical compounds, agrochemicals, and specialty chemicals. Its reactivity allows for the introduction of functional groups at specific positions, making it highly valuable in the design and production of new molecules with desired properties. Additionally, this compound can undergo different transformations, such as oxidation, reduction, and substitution reactions, to yield a diverse array of derivatives.Furthermore, 1-Propanone, 3-hydroxy-1-phenyl- serves as a starting material for the preparation of chiral compounds, which are essential in the production of enantiopure drugs and fine chemicals. By utilizing this intermediate in asymmetric synthesis, chemists can access enantiomerically pure products with high selectivity and efficiency. This ability to control the stereochemistry of the final products is crucial in drug discovery and the development of advanced materials with specific functionalities.
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