Molecular structure of 1-Phenyl-3-buten-1-ol, CAS Number: 936-58-3
1-Phenyl-3-buten-1-ol (CAS 936-58-3)
Alternate Names:
4-Phenyl-1-buten-4-ol
CAS Number:
936-58-3
Molecular Weight:
148.20
Molecular Formula:
C10H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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1-Phenyl-3-buten-1-ol is a key component in the biosynthesis of various natural products. It plays a role in the formation of secondary metabolites, which are important for the survival and adaptation of plants in their environment. 1-Phenyl-3-buten-1-ol is involved in the production of phytoalexins, which are defense compounds that protect plants from pathogens and pests. 1-Phenyl-3-buten-1-ol is a precursor in the biosynthesis of various volatile organic compounds that contribute to the characteristic aroma of certain plants. Its role in plant biochemistry highlights its significance in ecological interactions and the adaptation of plants to their surroundings.
1-Phenyl-3-buten-1-ol (CAS 936-58-3) References
- Enzymatic resolution of homoallyllic alcohols using various Rhizopus species. | Salvi, NA., et al. 2003. Biotechnol Lett. 25: 1081-6. PMID: 12889818
- Homoallylic alcohol isomerization in water over an immobilized Ru(II) organometallic catalyst with mesoporous structure. | Li, H., et al. 2006. J Phys Chem B. 110: 22942-6. PMID: 17092048
- Immobilization of Ru(II) complex on functionalized SBA-15 and its catalytic performance in aqueous homoallylic alcohol isomerization | Ying Wan a, Fang Zhang a, Yunfeng Lu b, Hexing Li a. 2007. Journal of Molecular Catalysis A: Chemical. 267: 165-172.
- Lanthanide–surfactant-combined catalysts for the allylation of benzaldehyde with tetraallyltin in aqueous solutions | Karen Deleersnyder, Danzhao Shi, Koen Binnemans, Tatjana N. Parac-Vogt. 2008. Journal of Alloys and Compounds. 451: 418-421.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Phenyl-3-buten-1-ol, 5 g | sc-252192 | 5 g | $88.00 |