| CAS ID | 7151-68-0 |
|---|---|
| IUPAC Name | 3-methoxy-4-methylbenzoic acid |
| Molecular Formula | C9H10O3 |
| Molecular Weight | |
| SMILES | COC1=CC(=CC=C1C)C(O)=O |
| CAS ID | 7151-68-0 |
|---|---|
| IUPAC Name | 3-methoxy-4-methylbenzoic acid |
| Molecular Formula | C9H10O3 |
| Molecular Weight | |
| SMILES | COC1=CC(=CC=C1C)C(O)=O |
| 81579 |
Synonym: 4-methyl-m-anisic acid, 3-methoxy-p-toluic acid, benzoic acid, 3-methoxy-4-methyl, 3-methoxy-4-methyl-benzoic acid, 3-methoxy-4-methyl benzoic acid, 3-methoxy-p-toluic acid; 4-methyl-m-anisic acid, 3-methoxy-4-methylbenzoicacid, pubchem2672, 5-carboxy-2-methylanisole, acmc-209oj0
| Color | White |
| Formula Weight | 166.18 |
| Physical Form | Crystal-Powder at 20°C |
| Chemical Name or Material | 3-Methoxy-4-methylbenzoic Acid |
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The aromatic carboxylic acid family includes the chemical compound 3-Methoxy-4-methyl benzoic acid. The presence of a carboxylic acid (-COOH) functional group, a benzene ring, and methyl and methoxy groups on the ring are the defining features of this compound. Chemical synthesis and pharmacological intermediates are only two of the many uses made possible by its unique structural arrangement.
There are several ways to produce 3-Methoxy-4-methyl benzoic acid, including: Methylation is the process of adding a methoxy group to the benzene ring, then methylating and carboxylation it. Aromatic precursors containing methyl groups oxidized. Enhanced yield and purity were achieved with the application of state-of-the-art catalytic methods.
The chemical has many applications: These are used in the compounding and manufacturing of drugs. The agricultural sector uses it as a chemical building block for agrochemicals. The production of aromatic compounds is an essential step in the chemical industry. Useful for academic research on aromatic acid reactivity and derivatives.
Indeed, manufacturers frequently provide bespoke synthesis services to meet specific needs, such as modifying the compound's purity, particle size, or functional groups, which is very useful in research and commercial settings.
Its unusual structure—a benzene ring with a methoxy and methyl group—affects reactivity and solubility. For some reactions, its superior performance and yield make it the compound of choice.
