942-58-5

Basic information

• Product Name: 1-(1-methylethyl)-2-(2-propen-1-yloxy)benzene
• Synonyms: 1-(1-methylethyl)-2-(2-propen-1-yloxy)benzene
• CAS NO: 942-58-5
• Molecular Weight: 176.258
• Mol File: 942-58-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(1-methylethyl)-2-(2-propen-1-yloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-methylethyl)-2-(2-propen-1-yloxy)benzene(942-58-5)
• EPA Substance Registry System: 1-(1-methylethyl)-2-(2-propen-1-yloxy)benzene(942-58-5)

Safety Data

• Hazardous Substances Data: 942-58-5(Hazardous Substances Data)

Upstream product

• 88-69-7 2-(1-methylethyl)phenol 
• 107-05-1 3-chloroprop-1-ene 

Downstream Products

• 1610349-70-6 (E)-cinnamyl 2-isopropylphenyl ether 
• 1610349-82-0 (E)-2-[3-(2-isopropylphenoxy)-1-propen-1-yl]thiophene 
• 1610349-88-6 (E)-1-[3-(2-isopropylphenoxy)-2-propen-1-yl]naphthalene 
• 88-69-7 2-(1-methylethyl)phenol 
• 3354-56-1 2-allyl-6-isopropylphenol 
• 74663-48-2 2-(1-methylethyl)-6-propylphenol 

Relevant articles and documents

An efficient palladium-catalyzed synthesis of cinnamyl ethers from aromatic halides, phenols, and allylic chloride

A one-pot, two-step catalytic protocol for the preparation of cinnamyl ethers from simple and readily available aryl halides, phenols and allyl chloride is reported for the first time. This simple and highly efficient palladium nanoparticles catalytic system shows good regio- and stereoselectivities and affords the desired products in good to high yields (49-85%) from aryl iodides. Furthermore, less reactive aryl bromides can also give the cinnamyl ethers in moderate yields (24-72%).