AH17133
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $13.00 | $10.00 | - + | |
1g | 98% | in stock | $47.00 | $33.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AH17133 |
Chemical Name: | 3-Hydroxy-2-methoxybenzaldehyde |
CAS Number: | 66495-88-3 |
Molecular Formula: | C8H8O3 |
Molecular Weight: | 152.14731999999998 |
MDL Number: | MFCD06656119 |
SMILES: | COc1c(C=O)cccc1O |
Complexity: | 135 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
XLogP3: | 1 |
3-Hydroxy-2-methoxybenzaldehyde, also known as vanillin alcohol, is a versatile compound widely used in chemical synthesis. Its unique structure makes it a valuable building block in the production of various pharmaceuticals, fragrances, and flavorings.1. Amidation Reactions: 3-Hydroxy-2-methoxybenzaldehyde can undergo amidation reactions to produce amides, which are important intermediates in the synthesis of pharmaceutical compounds.2. Oxidation Reactions: Due to its phenolic group, this compound can be easily oxidized to form corresponding carboxylic acids or other functional groups, expanding its utility in organic synthesis.3. Mannich Reactions: The aldehyde group in 3-Hydroxy-2-methoxybenzaldehyde is reactive and can participate in Mannich reactions to yield β-amino alcohols, which are key structural motifs in drug discovery and development.In summary, 3-Hydroxy-2-methoxybenzaldehyde is a valuable compound in chemical synthesis due to its ability to participate in various reactions and serve as a precursor for the production of diverse organic compounds.
Bioorganic & medicinal chemistry 20090415