Molecular structure of 3-Methoxycatechol, CAS Number: 934-00-9
3-Methoxycatechol (CAS 934-00-9)
Alternate Names:
1,2-Dihydroxy-3-methoxybenzene; 3-Methoxypyrocatechol; Pyrogallol monomethyl ether
CAS Number:
934-00-9
Purity:
98%
Molecular Weight:
140.14
Molecular Formula:
CH3OC6H3(OH)2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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3-Methoxycatechol functions as a substrate in enzymatic reactions, particularly in the field of biochemistry and molecular biology. It serves as a precursor in the synthesis of various organic compounds, playing a role in the formation of complex molecules. At the molecular level, 3-Methoxycatechol interacts with specific enzymes and proteins, influencing their activity and contributing to the biochemical processes. Its mechanism of action involves binding to active sites and participating in chemical reactions that lead to the production of desired compounds. 3-Methoxycatechol′s function in experimental applications involves its involvement in the manipulation of biological pathways and the study of enzymatic mechanisms, providing insights into the fundamental processes of cellular function and metabolism.
3-Methoxycatechol (CAS 934-00-9) References
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- Hot-hole extraction from quantum dot to molecular adsorbate. | Singhal, P. and Ghosh, HN. 2015. Chemistry. 21: 4405-12. PMID: 25656635
- Catechols as Sources of Hydrogen Atoms in Radical Deiodination and Related Reactions. | Povie, G., et al. 2016. Angew Chem Int Ed Engl. 55: 11221-5. PMID: 27392329
- Catalytic Cleavage of the C-O Bond in 2,6-dimethoxyphenol Without External Hydrogen or Organic Solvent Using Catalytic Vanadium Metal. | Yu, P., et al. 2020. Front Chem. 8: 636. PMID: 32850653
- Conversion of lignin-derived 3-methoxycatechol to the natural product purpurogallin using bacterial P450 GcoAB and laccase CueO. | Zhang, S., et al. 2022. Appl Microbiol Biotechnol. 106: 593-603. PMID: 34971410
- Structure-dependent antiviral activity of catechol derivatives in pyroligneous acid against the encephalomycarditis virus. | Li, R., et al. 2018. RSC Adv. 8: 35888-35896. PMID: 35558500
- Single-Site Mutation Induces Water-Mediated Promiscuity in Lignin Breaking Cytochrome P450GcoA. | Singh, W., et al. 2022. ACS Omega. 7: 21109-21118. PMID: 35755387
- Oxidation of Catechols at the Air-Water Interface by Nitrate Radicals. | Rana, MS. and Guzman, MI. 2022. Environ Sci Technol. 56: 15437-15448. PMID: 36318667
- Effects of combined treatment with phenolic compounds and sodium nitrite on two-stage carcinogenesis and cell proliferation in the rat stomach. | Kawabe, M., et al. 1994. Jpn J Cancer Res. 85: 17-25. PMID: 8106288
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Methoxycatechol, 5 g | sc-231804 | 5 g | $77.00 |