6397-77-9

Basic information

• Product Name: Benzene, 1,1'-(diethoxymethylene)bis-
• CAS NO: 6397-77-9
• Molecular Formula: C17H20O2
• Molecular Weight: 256.345
• Mol File: 6397-77-9.mol
• Article Data: 12

Chemical Properties

• Melting Point: 51-51.5 °C
• Boiling Point: 323.673oC at 760 mmHg
• Flash Point: 111.452oC
• Density: 1.032g/cm3
• CAS DataBase Reference: Benzene, 1,1'-(diethoxymethylene)bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(diethoxymethylene)bis-(6397-77-9)
• EPA Substance Registry System: Benzene, 1,1'-(diethoxymethylene)bis-(6397-77-9)

Safety Data

• Hazardous Substances Data: 6397-77-9(Hazardous Substances Data)

Upstream product

• 2051-90-3 Dichlorodiphenylmethane 
• 141-52-6 sodium ethanolate 
• 119-61-9 benzophenone 
• 122-51-0 orthoformic acid triethyl ester 
• 64-17-5 ethanol 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 7500-79-0 N-methyl-diphenyl-nitrone 
• 3784-21-2 1,2-diethoxy-1,1,2,2-tetraphenylethane 
• 876485-66-4 bis-(α-ethoxy-benzhydryl)-peroxide 
• 15568-75-9 3-(4-nitro-phenyl)-5,5-diphenyl-[1,4,2]dioxazole 
• 15568-71-5 3,5,5-triphenyl-[1,4,2]dioxazole 
• 46498-57-1 Ethoxy-diphenyl-carbonium 
• 6317-10-8 2,2-diphenyl-1,3-dithiolane 
• 15568-79-3 3-(4-chloro-phenyl)-5,5-diphenyl-[1,4,2]dioxazole 

Relevant articles and documents

Practical acetalization and transacetalization of carbonyl compounds catalyzed by recyclable PVP-I

A novel PVP-I catalyzed acetalizations/transacetalizations of carbonyl compounds has been developed processing with a mild and easy handling fashion. Different types of Acyclic and cyclic acetals were prepared from carbonyl compounds or their acetals successfully. Further applications of newly developed catalytic combination were testified. This protocol featured with simplicity of operation, mild reaction condition, short reaction time, recyclable of catalyst and broad substrates scope with excellent yields.

Iron(III) tosylate in the preparation of dimethyl and diethyl acetals from ketones and β-keto enol ethers from cyclic β-diketones

An efficient method for conversion of ketones to their corresponding dimethyl and diethyl acetals and of cyclic β-diketones into β-keto enol ethers using Fe(OTs)3 as a catalyst is described. Copyright Taylor & Francis Group, LLC.

Simple method for the preparation of dimethyl acetals from ketones with montmorillonite K 10 and p-toluenesulfonic acid

A simple method for conversion of ketones to their corresponding dimethyl acetals using montmorillonite K 10 and p-toluenesulfonic acid as acidic cocatalysts under very mild reaction conditions is described. Copyright Taylor & Francis Group, LLC.