2-Hydroxybenzyl alcohol (CAS 90-01-7)
QUICK LINKS
2-Hydroxybenzyl alcohol is extensively studied in the field of organic chemistry due to its role as a precursor in the synthesis of various pharmaceutical and chemical compounds. Researchers explore its reactivity and transformations under different conditions to optimize synthesis pathways and enhance yields of target molecules. The compound′s ability to participate in various chemical reactions, such as esterification and etherification, makes it a valuable subject in the development of complex chemical architectures. Additionally, 2-Hydroxybenzyl alcohol is investigated for its potential as a natural antioxidant, focusing on its capacity to scavenge reactive oxygen species and reduce oxidative stress. The studies also delve into its photoprotective properties, examining how it absorbs and dissipates ultraviolet radiation, which is relevant in cosmetic and dermatological applications.
2-Hydroxybenzyl alcohol (CAS 90-01-7) References
- Ca2+ assisted glycosylation of phenolic compounds by phenolic-UDP-glycosyltransferase from Bacillus subtilis PI18. | Li, B., et al. 2019. Int J Biol Macromol. 135: 373-378. PMID: 31108143
- Characterisation, release and migration of phenolic compounds from resoles used in polyester-phenol coatings intended for food contact materials. | Eckardt, M., et al. 2020. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 37: 1791-1810. PMID: 32706303
- Enzymatic Synthesis of Lipophilic Esters of Phenolic Compounds, Evaluation of Their Antioxidant Activity and Effect on the Oxidative Stability of Selected Oils. | Zieniuk, B., et al. 2021. Biomolecules. 11: PMID: 33669574
- A thermostable glycosyltransferase from Paenibacillus polymyxa NJPI29: recombinant expression, characterization, and application in synthesis of glycosides. | Chang, S., et al. 2021. 3 Biotech. 11: 314. PMID: 34109099
- Catalytic Acceptorless Dehydrogenation of Amino Alcohols and 2-Hydroxybenzyl Alcohols for Annulation Reaction under Neutral Conditions. | Pandey, AM., et al. 2021. J Org Chem. 86: 8805-8828. PMID: 34151556
- A Fungal Versatile GH10 Endoxylanase and Its Glycosynthase Variant: Synthesis of Xylooligosaccharides and Glycosides of Bioactive Phenolic Compounds. | Pozo-Rodríguez, A., et al. 2022. Int J Mol Sci. 23: PMID: 35163307
- Effects of salicylate derivatives on localization of p.H723R allele product of SLC26A4. | Murakoshi, M., et al. 2022. Auris Nasus Larynx. 49: 928-937. PMID: 35305848
- Design, step-economical diversity-oriented synthesis of an N-heterocyclic library containing a pyrimidine moiety: discovery of novel potential herbicidal agents. | Ma, D., et al. 2021. RSC Adv. 11: 15380-15386. PMID: 35424046
- Electrochemical synthesis of quinazolinone via I2-catalyzed tandem oxidation in aqueous solution. | Hou, H., et al. 2021. RSC Adv. 11: 17721-17726. PMID: 35480173
- Photochemical Synthesis of the Bioactive Fragment of Salbutamol and Derivatives in a Self-Optimizing Flow Chemistry Platform. | Gérardy, R., et al. 2022. Chemistry. 28: e202201385. PMID: 35570196
- Overexpression of dihydroflavonol 4-reductase (CoDFR) boosts flavonoid production involved in the anthracnose resistance. | Yang, C., et al. 2022. Front Plant Sci. 13: 1038467. PMID: 36438122
- Self-Healing Alginate Hydrogel Formed by Dynamic Benzoxaborolate Chemistry Protects Retinal Pigment Epithelium Cells against Oxidative Damage. | Liu, M., et al. 2022. Gels. 9: PMID: 36661792
- Season, storage and extraction method impact on the phytochemical profile of Terminalia ivorensis. | Moomin, A., et al. 2023. BMC Plant Biol. 23: 162. PMID: 36964494
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Hydroxybenzyl alcohol, 25 g | sc-238079 | 25 g | $46.00 |