64047-87-6

Basic information

• Product Name: 2,6-Diallyl-4-methoxyphenol
• Synonyms: 2,6-Diallyl-4-methoxyphenol
• CAS NO: 64047-87-6
• Molecular Formula: C₁₃H₁₆O₂
• Molecular Weight: 204.2649
• Mol File: 64047-87-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 316°Cat760mmHg
• Flash Point: 142.7°C
• Appearance: /
• Density: 1.017g/cm³
• Vapor Pressure: 0.000228mmHg at 25°C
• Refractive Index: 1.536
• CAS DataBase Reference: 2,6-Diallyl-4-methoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Diallyl-4-methoxyphenol(64047-87-6)
• EPA Substance Registry System: 2,6-Diallyl-4-methoxyphenol(64047-87-6)

Safety Data

• Hazardous Substances Data: 64047-87-6(Hazardous Substances Data)

Usage

General Description

2,6-Diallyl-4-methoxyphenol, also known as eugenol, is a chemical compound found in various essential oils such as clove oil, cinnamon oil, and basil oil. It has a strong, pleasant odor and is commonly used as a flavoring agent and fragrance in perfumes and cosmetics. Eugenol has been shown to have antimicrobial, antioxidant, and anti-inflammatory properties, making it a popular ingredient in traditional medicine and natural remedies. It also has analgesic properties and is often used in dental products for its numbing effect. Additionally, eugenol has been studied for its potential as an insecticide and herbicide. However,

InChI:InChI=1/C13H16O2/c1-4-6-10-8-12(15-3)9-11(7-5-2)13(10)14/h4-5,8-9,14H,1-2,6-7H2,3H3

Upstream product

• 205433-77-8 2-allyl-1-allyloxy-4-methoxy-benzene 
• 13391-35-0 allyl (4-methoxyphenyl) ether 
• 584-82-7 2-allyl-4-methoxyphenol 
• 150-76-5 4-methoxy-phenol 
• 123-31-9 hydroquinone 

Downstream Products

• 141989-06-2 4-methoxy-2,6-dipropylphenol 
• 141988-91-2 4,4-dimethoxy-2,6-dipropyl-2,5-cyclohexadienone 
• 1262758-84-8 C₂₇H₃₂O₆ 
• 1262758-85-9 C₂₃H₂₈O₄ 
• 1262758-96-2 C₂₅H₃₂O₈S₂ 
• 1262758-86-0 C₂₃H₂₆Br₂O₂ 
• 1262758-87-1 C₂₂H₂₄Br₂O₂ 
• 1262758-88-2 C₂₃H₂₆Br₂O₃ 
• 1262758-94-0 C₁₆H₂₂O₄ 
• 1262758-81-5 C₁₆H₂₀Br₂O₂ 
• 1262758-95-1 C₁₅H₁₈Br₂O₂ 
• 1262758-82-6 C₁₆H₂₀Br₂O₃ 
• 1262758-80-4 C₂₀H₂₆O₆ 
• 67903-03-1 2,6-di(3-methyl-2-butenyl)benzene-1,4-diol 

Relevant articles and documents

Allylphenols as a new class of human 15-lipoxygenase-1 inhibitors

In this study, a series of mono- and diallylphenol derivative were designed, synthesized, and evaluated as potential human 15-lipoxygenase-1 (15-hLOX-1) inhibitors. Radical scavenging potency of the synthetic allylphenol derivatives was assessed and the results were in accordance with lipoxygenase (LOX) inhibition potency. It was found that the electronic natures of allyl moiety and para substituents play the main role in radical scavenging activity and subsequently LOX inhibition potency of the synthetic inhibitors. Among the synthetic compounds, 2,6-diallyl-4-(hexyloxy)phenol (42) and 2,6-diallyl-4-aminophenol (47) showed the best results for LOX inhibition (IC50 = 0.88 and 0.80 μM, respectively).

Photochemistry of Substituted 4,4-Dimethoxy-2,5-Cyclohexadienones

4,4-Dimethoxy-2,5-cyclohexadienones 9-14 were prepared from the corresponding hydroquinone monomethyl ethers by oxidation with thallium trinitrate in methanol. Irradiation of solutions of 9-13 in methanol with a broad band of UV light centered at 350 nm in a Rayonet reactor afforded 2-cyclopentenone derivatives 15-19 in moderate to excellent yields, whereas irradiation of 14 in methanol gave phenol 8 along with other unidentified products. Irradiation of 11-14 in benzene yielded substituted phenols. The plausible reaction pathways for the product formation are discussed.