3864-15-1

Basic information

• Product Name: Benzeneethanol, a-(3,4-dimethoxyphenyl)-
• CAS NO: 3864-15-1
• Molecular Formula: C16H18O3
• Molecular Weight: 258.317
• Mol File: 3864-15-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzeneethanol, a-(3,4-dimethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanol, a-(3,4-dimethoxyphenyl)-(3864-15-1)
• EPA Substance Registry System: Benzeneethanol, a-(3,4-dimethoxyphenyl)-(3864-15-1)

Safety Data

• Hazardous Substances Data: 3864-15-1(Hazardous Substances Data)

Upstream product

• 1589-82-8 phenylmagnesium bromide 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 103-80-0 phenylacetyl chloride 
• 91-16-7 1,2-dimethoxybenzene 
• 103-82-2 phenylacetic acid 
• 100-44-7 benzyl chloride 
• 3141-93-3 4',5'-dimethoxydeoxybenzoin 

Downstream Products

• 79997-18-5 1-(3,4-dimethoxyphenyl)-2-phenylethane-1,2-dione 
• 3141-93-3 4',5'-dimethoxydeoxybenzoin 
• 106053-66-1 2-<2-(4-acetylphenyl)-ethyl>-4,5-dimethoxy-acetophenon 
• 106053-65-0 4,5-Dimethoxy-2-(2-phenylethyl)acetophenon 
• 140-11-4 Benzyl acetate 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 3892-93-1 1-(3,4-dimethoxyphenyl)-2-phenylethane 

Relevant articles and documents

An unusual chemoselective oxidation strategy by an unprecedented exploration of an electrophilic center of DMSO: A new facet to classical DMSO oxidation

A conceptually new dimethyl sulfoxide (DMSO) based oxidation process without the use of any activator has been demonstrated for the oxidation of active methylenes and benzhydrols. The developed protocol utilizes the electrophilic center of DMSO for oxidation, which was unexplored before. Mechanistic investigation has confirmed that the source of oxygen is DMSO.

Syntheses og Stilbenes with a C2-Sidechain in o-Position and of their Deuteriated Analogues

Syntheses of o-(β-aminoethyl)-stilbene-urethanes (types 1, 2 and 3) and o-(β-phenethyl)-stilbenes 4 are described.The urethanes are obtained by degradation of 1-benzyl-1,2,3,4-tetrahydroisoquinolines with ethylchloroformate; 4 is synthesized by reduction of desoxybenzoines, followed by o-formylation and Wittig-reaction.The deuteriated isotopomers were obtained via the corresponding deuteriated precursors. - Keywords: Stilbenes, o-substituted; Deuteriated compounds