16215-47-7

Basic information

• Product Name: Benzene, 1-ethenyl-4-(2-propenyloxy)-
• CAS NO: 16215-47-7
• Molecular Formula: C11H12O
• Molecular Weight: 160.216
• Mol File: 16215-47-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1-ethenyl-4-(2-propenyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-ethenyl-4-(2-propenyloxy)-(16215-47-7)
• EPA Substance Registry System: Benzene, 1-ethenyl-4-(2-propenyloxy)-(16215-47-7)

Safety Data

• Hazardous Substances Data: 16215-47-7(Hazardous Substances Data)

Usage

General Description

Benzene, 1-ethenyl-4-(2-propenyloxy)- is a chemical compound with a molecular formula C16H16O. It is a type of aromatic compound with a benzene ring and attached ethenyl and propenyloxy groups. Benzene, 1-ethenyl-4-(2-propenyloxy)- is used in the synthesis of various organic compounds including polymers, resins, and pharmaceuticals. It is also used as an intermediate in the production of dyes and perfumes. Benzene, 1-ethenyl-4-(2-propenyloxy)- is considered to be a potentially hazardous chemical and should be handled with care and used in controlled environments.

Upstream product

• 2628-17-3 4-Vinylphenol 
• 106-95-6 allyl bromide 
• 75175-10-9 4-benzoyloxy-trans-cinnamic acid 
• 40663-68-1 4-(2-propenyloxy)benzaldehyde 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 123-08-0 4-hydroxy-benzaldehyde 
• 2628-16-2 p-acetoxystyrene 
• 32568-59-5 4-vinylphenyl benzoate 
• 5339-06-0 4-formylphenyl benzoate 

Downstream Products

• 149738-31-8 3-(4-vinylphenyloxy)propyl trimethoxysilane 
• 1369494-79-0 (Z)-1-allyloxy-4-(prop-1-en-1-yl)benzene 
• 305815-25-2 (E)-1-(allyloxy)-4-(prop-1-en-1-yl)benzene 
• 40663-68-1 4-(2-propenyloxy)benzaldehyde 
• 3585-67-9 2-(4-Allyloxy-phenyl)-propan-1-ol 
• 99859-60-6 [4-(1,2-dibromo-ethyl)-phenyl]-(2,3-dibromo-propyl)-ether 

Relevant articles and documents

Copper(ii)-catalyzed protoboration of allenes in aqueous media and open air

A method has been developed for the facile Cu(ii)-catalyzed protoboration of monosubstituted allenes in aqueous media under atmospheric conditions. The reaction occurs site selectively, favoring internal alkene protoboration to afford 1,1-disubstituted vinylboronic acid derivatives (up to 93?:?7) with modest to good yields. The method has been applied to a variety of phenylallene derivatives as well as alkyl-substituted allenes. This journal is

Expanding the regioselective enzymatic repertoire: Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta

The first report of a biocatalytic regioselective oxidative mono-cleavage of dialkenes was successfully achieved employing a cell-free enzyme preparation from Trametes hirsuta at the expense of molecular oxygen. Selected reactions were performed on a preparative scale affording high to excellent conversions and chemoselectivities. The Royal Society of Chemistry 2012.

Method for production of allyloxystyrene compounds

Allylic styrene ether compounds of the formula: STR1 where R1 is an optionally substituted allylic or propargyl hydrocarbon group, and R2, R3, and R4 are independently H, C1-6 hydrocarbon or C1-6