35237-02-6

Basic information

• Product Name: 1,2-Benzenediol, 3-(8Z)-8-pentadecenyl-
• CAS NO: 35237-02-6
• Molecular Formula: C21H34O2
• Molecular Weight: 318.5
• Mol File: 35237-02-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-Benzenediol, 3-(8Z)-8-pentadecenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenediol, 3-(8Z)-8-pentadecenyl-(35237-02-6)
• EPA Substance Registry System: 1,2-Benzenediol, 3-(8Z)-8-pentadecenyl-(35237-02-6)

Safety Data

• Hazardous Substances Data: 35237-02-6(Hazardous Substances Data)

Usage

General Description

1,2-Benzenediol, 3-(8Z)-8-pentadecenyl- is a chemical compound that is also known as alpha-terpineol. It is a colorless liquid with a pleasant, lilac-like odor and is commonly found in a variety of natural sources, including pine oil, orange peel, and other essential oils. It has a wide range of applications, including use as a fragrance ingredient in perfumes and cosmetics, as a flavoring agent in food products, and as an intermediate in the synthesis of other organic compounds. It is also used in the production of pharmaceuticals and as a solvent in various industrial processes. Alpha-terpineol has potential health effects and has been shown to exhibit antimicrobial, anti-inflammatory, and antioxidant properties.

Upstream product

• 123-99-9 azelaic acid 
• 76035-43-3 1,2-dimethoxy-3-<(Z)-pentadec-8-enyl>benzene 
• 76014-94-3 3-(pentadec-8-ynyl)veratrole 
• 4549-31-9 1,7-dibromoheptane 
• 53545-40-7 1-(2,3-dimethoxy-phenyl)-7-(1-ethoxy-ethoxy)-heptan-1-ol 
• 53545-42-9 7-(2,3-dihydroxyphenyl)heptyl bromide 
• 86-51-1 2,3-dimethyoxybenzaldehyde 
• 51732-22-0 acetaldehyde ethyl 6-chlorohexyl acetal 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 21433-45-4 1-octynyllithium 
• 76014-93-2 1-bromo-7-(2,3-dimethoxyphenyl)heptane 
• 59340-54-4 1-(2,3-dimethoxyphenyl)heptane-1,7-diol 
• 53545-41-8 7-(2,3-dimethoxyphenyl)heptan-1-ol 
• 2009-83-8 6-chloro-1-hexanol 

Downstream Products

• 492-89-7 3-pentadecylcatechol 
• 72955-56-7 1,2-diacetoxy-3-pentadec-8-enyl-benzene 
• 76035-43-3 1,2-dimethoxy-3-<(Z)-pentadec-8-enyl>benzene 
• 73881-19-3 1,2-diacethyl-3-pentadecylbenzene 

Relevant articles and documents

Application of benzyl protecting groups in the synthesis of prenylated aromatic compounds

Benzyl ethers have proven to be useful protecting groups for synthesis of phenols bearing isoprenoid chains because the benzyl groups can tolerate the conditions of halogen-metal exchange used to introduce the side chains yet are cleaved in good yields upon treatment with sodium s-butanol.

Vesicant Principles of Poison Ivy and Related Plants: Synthesis of the Urushiols, 1,2-Dihydroxy-3-benzene and 1,2-Dihydroxy-3-pentadecylbenzene

New syntheses of 1,2-dihydroxy-3-benzene (1) and 1,2-dihydroxy-3-pentadecylbenzene (4), vesicant principles of Poison Ivy (Rhus radicans) and other species of Anacardiaceae, are described starting from 1,2-dimethoxybenzene (7).The lithiation of 1,2-dimethoxybenzene (7) has been re-examined and the yield of the product, 2,3-dimethoxyphenyl-lithium (8), re-determined.The reaction of the aryl-lithium with 1,7-dibromoheptane has been studied by g.l.c., using tributyltin chloride as a quenching reagent.The extracts of two plants of the Anacardiaceae family, Semecarpus vitiensis Engl. and Melanorrhoea beccari Engl., have been examined for the presence of urushiols.The bark of the latter has been found to contain gallic acid.