1005-40-9

Basic information

• Product Name: Benzene, 1-(ethenyloxy)-3-methyl-
• CAS NO: 1005-40-9
• Molecular Formula: C9H10O
• Molecular Weight: 134.178
• Mol File: 1005-40-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(ethenyloxy)-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(ethenyloxy)-3-methyl-(1005-40-9)
• EPA Substance Registry System: Benzene, 1-(ethenyloxy)-3-methyl-(1005-40-9)

Safety Data

• Hazardous Substances Data: 1005-40-9(Hazardous Substances Data)

Upstream product

• 75-01-4 chloroethylene 
• 3019-89-4 sodium 3-methylphenoxide 
• 74-85-1 ethene 
• 108-39-4 3-methyl-phenol 
• 106-93-4 ethylene dibromide 
• 74-86-2 acetylene 
• 107-06-2 1,2-dichloro-ethane 

Downstream Products

• 34573-90-5 1,1,2,2-Tetracyano-3-(3'-methyl)-phenoxycyclobutan 
• 93534-35-1 1,2,3,4,7,7-Hexachlor-5-m-tolyloxy-bicyclo<2.2.1>hepten-(2) 
• 111862-28-3 1-(1-Chloro-2-thiocyanato-ethoxy)-3-methyl-benzene 
• 137711-34-3 2-Chloro-2-m-tolyloxy-ethanesulfonyl fluoride 
• 3406-89-1 m-Tolyl-<2-phenylmercapto-vinyl>-ether 
• 137711-37-6 (E)-2-m-Tolyloxy-ethenesulfonyl fluoride 
• 111862-34-1 1-Methyl-3-((E)-2-thiocyanato-vinyloxy)-benzene 
• 1369970-21-7 1-(3-methylphenoxy)ethyl bis[2-(2-furyl)ethyl]phosphinodiselenoate 
• 1369970-19-3 1-(3-methylphenoxy)ethyl bis[2-(4-methoxyphenyl)ethyl]phosphinodiselenoate 
• 63053-30-5 1-Chlor-2-phenylsulfonylethyl-m-tolylether 
• 111862-23-8 1-(1,2-Bis-thiocyanato-ethoxy)-3-methyl-benzene 
• 53552-42-4 2-m-tolyloxy-propionaldehyde 
• 18928-82-0 1-m-Tolyloxy-2-dichlor-cyclopropan 
• 18928-87-5 1-Cyclopropoxy-3-methyl-benzene 

Relevant articles and documents

Polymer-supported β-bromoethyl selenide: An efficient reagent for the synthesis of aryl vinyl ethers

A simple and efficient procedure for the solid-phase synthesis of aryl vinyl ethers using polymer-supported β-bromoethyl selenide with traceless linker strategy is described.

-

-

Nucleophilic addition to acetylenes in superbasic catalytic systems: XVIII. Vinylation of phenols and naphthols with acetylene

Phenols and naphthols react with acetylene in a superbasic system KOH-DMSO forming the corresponding aryl vinyl ethers in up to 80% yields.

β-Phenylselenoethanol, an efficient reagent for the one-pot synthesis of aryl vinyl ethers

β-Phenylselenoethanol was treated with phenols under Mitsunobu conditions and subsequent oxidation-elimination with 30% hydrogen peroxide furnished aryl vinyl ethers with good yields (85-90%) in a one-pot, two-step transformation.