3727-20-6

Basic information

• Product Name: 1,4-dimethyl-2-(prop-2-en-1-yloxy)benzene
• CAS NO: 3727-20-6
• Molecular Formula: C₁₁H₁₄O
• Molecular Weight: 162.2283
• Mol File: 3727-20-6.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 236.2°C at 760 mmHg
• Flash Point: 87.8°C
• Density: 0.931g/cm³
• Vapor Pressure: 0.0735mmHg at 25°C
• Refractive Index: 1.504
• CAS DataBase Reference: 1,4-dimethyl-2-(prop-2-en-1-yloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dimethyl-2-(prop-2-en-1-yloxy)benzene(3727-20-6)
• EPA Substance Registry System: 1,4-dimethyl-2-(prop-2-en-1-yloxy)benzene(3727-20-6)

Safety Data

• Hazardous Substances Data: 3727-20-6(Hazardous Substances Data)

Usage

Family

Phenylpropanoids

Source

Derived from essential oils of plants such as nutmeg, ylang-ylang, and clove

Uses

a. Perfumery and flavoring due to its sweet, woody, and spicy aroma
b. Dental and oral care products due to its antiseptic and anti-inflammatory properties
c. Pharmaceutical formulations

Safety concerns

a. Skin irritant and sensitizer
b. Can cause allergic reactions in some individuals
c. Should be used with caution and according to proper safety guidelines

Upstream product

• 132907-18-7 3,6-dimethoxy-3,6-dimethylcyclohexa-1,4-diene 
• 107-18-6 allyl alcohol 
• 95-87-4 2,5-Dimethylphenol 
• 106-95-6 allyl bromide 
• 1200591-13-4 C₁₂H₁₄O₃ 
• 64-17-5 ethanol 
• 107-05-1 3-chloroprop-1-ene 

Downstream Products

• 126707-92-4 4,6-dimethyl-2-(phenylthiomethyl)-2,3-dihydrobenzofuran 
• 126707-91-3 4,7-dimethyl-2-(phenylthiomethyl)-2,3-dihydrobenzofuran 
• 126734-06-3 5-Chloro-4,6-dimethyl-2-phenylsulfanylmethyl-2,3-dihydro-benzofuran 
• 126734-05-2 5-Chloro-4,7-dimethyl-2-phenylsulfanylmethyl-2,3-dihydro-benzofuran 
• 126708-21-2 4,6-dimethyl-5-(phenylthio)-2-(phenylthiomethyl)-2,3-dihydrobenzofuran 
• 126708-20-1 4,7-dimethyl-5-(phenylthio)-2-(phenylthiomethyl)-2,3-dihydrobenzofuran 
• 3727-17-1 2-allyl-3,6-dimethylphenol 
• 104174-71-2 4-n-Propyl-2,5-dimethylphenol 
• 3727-16-0 2.5-Dimethyl-4-allyl-phenol 
• 95-87-4 2,5-Dimethylphenol 

Relevant articles and documents

Palladium-catalyzed anti-Markovnikov oxidative acetalization of activated olefins with iron(iii) sulphate as the reoxidant

This paper discloses the efficient palladium-catalyzed anti-Markovnikov oxidative acetalization of activated terminal olefins with iron(iii) sulfate as the reoxidant. This methodology requires mild reaction conditions and shows high regioselectivity toward anti-Markovnikov products and compatibility with a wide range of functional groups. Iron(iii) sulphate was the sole reoxidant used in this method. Various olefins like vinylarenes, aryl-allylethers, aryl or benzyl acrylates and homoallylic alcohols all reacted well providing anti-Markovnikov acetals, some of which represent orthogonally functionalized 1,3- and 1,4-dioxygenated compounds.

INDOLINE DERIVATIVES

Compounds of Formula (I) are disclosed and methods of treating viral infections with compositions comprising such compounds.

The sulfonation of methyl and prenyl ethers of naturally occurring phenols with trimethylsilylchlorosulfonate as sulfonating agent

At room temperature trimethylsilylchlorosulfonate has been found to be an effective and a mild reagent for the nuclear sulfonation of some methyl and prenyl ethers of naturally occurring phenols.