Molecular structure of 2,5-Dimethoxybenzyl alcohol, CAS Number: 33524-31-1
2,5-Dimethoxybenzyl alcohol (CAS 33524-31-1)
CAS Number:
33524-31-1
Molecular Weight:
168.19
Molecular Formula:
C9H12O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2,5-Dimethoxybenzyl alcohol is used as a self-indicating standard for assessing organolithium reagents. This compound has various applications within scientific research, functioning as a reagent in organic synthesis, a solvent for diverse reactions, and a substrate for enzyme assays. Moreover, it stands as a model compound in the studies of enzyme inhibition and functioning as a probe for the analysis of protein-protein interactions.
2,5-Dimethoxybenzyl alcohol (CAS 33524-31-1) References
- Structural effects on the OH-promoted fragmentation of methoxy-substituted 1-arylalkanol radical cations in aqueous solution: the role of oxygen acidity. | Baciocchi, E., et al. 2001. Chemistry. 7: 1408-16. PMID: 11330893
- Use of multiplex reverse transcription-PCR to study the expression of a laccase gene family in a basidiomycetous fungus. | González, T., et al. 2003. Appl Environ Microbiol. 69: 7083-90. PMID: 14660352
- Design, synthesis and biological evaluation of novel riccardiphenol analogs. | Kumar, SK., et al. 2005. Bioorg Med Chem. 13: 2873-80. PMID: 15781397
- Synthesis of new phytogrowth-inhibitory substituted aryl-p-benzoquinones. | de Almeida Barbosa, LC., et al. 2006. Chem Biodivers. 3: 553-67. PMID: 17193291
- Catalytic hypervalent iodine oxidation of p-dialkoxybenzenes to p-quinones using 4-iodophenoxyacetic acid and Oxone. | Yakura, T., et al. 2008. Chem Pharm Bull (Tokyo). 56: 1632-4. PMID: 18981622
- Mechanistic borderline of one-step hydrogen atom transfer versus stepwise Sc(3+)-coupled electron transfer from benzyl alcohol derivatives to a non-heme iron(IV)-oxo complex. | Morimoto, Y., et al. 2012. Inorg Chem. 51: 10025-36. PMID: 22954389
- Detection of glucose via enzyme-coupling reaction based on a DT-diaphorase fluorescence probe. | Gao, X., et al. 2014. Talanta. 120: 456-61. PMID: 24468396
- Acid-Triggered Colorimetric Hydrophobic Benzyl Alcohols for Soluble Tag-Assisted Liquid-Phase Synthesis. | Okada, Y., et al. 2015. Org Lett. 17: 4264-7. PMID: 26274781
- Chemical Composition, Antioxidant and Cytotoxic Activities of Essential Oil of the Inflorescence of Anacamptis coriophora subsp. fragrans (Orchidaceae) from Tunisia. | El Mokni, R., et al. 2016. Nat Prod Commun. 11: 857-60. PMID: 27534135
- Photoinitiating Systems Based on Anthraquinone Derivatives: Synthesis of Antifouling and Biocide Coatings. | Tomane, S., et al. 2017. Chempluschem. 82: 1298-1307. PMID: 31957991
- Traditional, Therapeutic Uses and Phytochemistry of Terrestrial European Orchids and Implications for Conservation. | Bazzicalupo, M., et al. 2023. Plants (Basel). 12: PMID: 36678970
- 2, 5-Dimethoxybenzyl alcohol: a convenient self-indicating standard for the determination of organolithium reagents | Winkle, M. R., Lansinger, J. M., & Ronald, R. C. 1980. Journal of the Chemical Society, Chemical Communications,. (3): 87-88.
- A formal synthesis of optically active clavicipitic acids, unusual azepinoindole-type ergot alkaloids | Shinohara, H., Fukuda, T., & Iwao, M. 1999. Tetrahedron. 55(36): 10989-11000.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2,5-Dimethoxybenzyl alcohol, 10 g | sc-238381 | 10 g | $87.00 |