Molecular structure of Methyl 2-hydroxy-3-methylbenzoate, CAS Number: 23287-26-5
Methyl 2-hydroxy-3-methylbenzoate (CAS 23287-26-5)
Alternate Names:
2-Hydroxy-3-methylbenzoic acid methyl ester; Methyl 3-methylsalicylate
CAS Number:
23287-26-5
Molecular Weight:
166.17
Molecular Formula:
C9H10O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Methyl 2-hydroxy-3-methylbenzoate involves the inhibition of specific enzymes, particularly cyclooxygenase-2 (COX-2). By targeting COX-2, this compound effectively hinders the production of prostaglandins, which are inflammatory molecules. Through this inhibition, Methyl 2-hydroxy-3-methylbenzoate can effectively alleviate inflammation and alleviate associated pain. By impeding the production of prostaglandins, this compound exerts its anti-inflammatory and analgesic effects.
Methyl 2-hydroxy-3-methylbenzoate (CAS 23287-26-5) References
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- Benzisothiazolinone Derivatives as Potent Allosteric Monoacylglycerol Lipase Inhibitors That Functionally Mimic Sulfenylation of Regulatory Cysteines. | Castelli, R., et al. 2020. J Med Chem. 63: 1261-1280. PMID: 31714779
- Spirocyclopropane compounds. III. Synthesis of spiro[benzofuran-2(3H),1'-cyclopropan]-3-ones for evaluation as gastric antisecretory and antiulcer agents. | Kawada, M., et al. 1984. Chem Pharm Bull (Tokyo). 32: 3532-50. PMID: 6525649
- Rate Acceleration of Nucleophilic Substitution of 2-Chloro-4,6-dimethoxypyrimidine by Sulfinate Catalysis | Y Bessard, R Crettaz. 2000. Tetrahedron. 56: 4739-4745.
- Pd(OAc)2-catalyzed orthogonal synthesis of 2-hydroxybenzoates and substituted cyclohexanones from acyclic unsaturated 1,3-carbonyl compounds | T Miyagi, S Okada, N Tada, M Sugihara, N Kagawa. 2019. Tetrahedron Letters. 60: 1653-1657.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Methyl 2-hydroxy-3-methylbenzoate, 2 g | sc-279341 | 2 g | $80.00 |