36234-10-3

Basic information

• Product Name: 3,3-DIETHOXY-1-PHENYL-1-PROPANONE
• Synonyms: 3,3-DIETHOXY-1-PHENYL-1-PROPANONE;3,3-DIETHOXY-1-PHENYL-PROPAN-1-ONE
• CAS NO: 36234-10-3
• Molecular Formula: C₁₃H₁₈O₃
• Molecular Weight: 0
• Mol File: 36234-10-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 320.234°C at 760 mmHg
• Flash Point: 138.495°C
• Appearance: /
• Density: 1.026g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.493
• CAS DataBase Reference: 3,3-DIETHOXY-1-PHENYL-1-PROPANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-DIETHOXY-1-PHENYL-1-PROPANONE(36234-10-3)
• EPA Substance Registry System: 3,3-DIETHOXY-1-PHENYL-1-PROPANONE(36234-10-3)

Safety Data

• Hazardous Substances Data: 36234-10-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H18O3/c1-3-15-13(16-4-2)10-12(14)11-8-6-5-7-9-11/h5-9,13H,3-4,10H2,1-2H3

Upstream product

• 64-17-5 ethanol 
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• 98-86-2 acetophenone 
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• 141-52-6 sodium ethanolate 
• 99647-88-8 1-phenyl-3-(methylnitroamino)-2-propen-1-one 
• 25438-37-3 phenyl(trimethylsiloxy)acetonitrile 
• 2032-35-1 Bromoacetaldehyde diethyl acetal 
• 827-36-1 2-(N,N-dimethylamino)-2-phenylacetonitrile 

Relevant articles and documents

THE FORMATION OF OPEN-CHAIN CARBOXONIUM AND CARBIMMONIUM IONS AND THEIR HETEROCYCLIZATION TO PYRYLIUM AND PYRIDINIUM CATIONS

During the action of an anhydrous solution of perchloric acid in alcohol on methyl aryl ketones in ethyl orthoformate open-chain carboxonium salts (derivatives of the 1,5-diaryl-2-pentene-1,5-dione) were formed instead of the 2,6-diarylpyrylium perchlorat

SOME PROPERTIES OF UNSATURATED NITROAMINES

In the reaction of ketovinylnitroamines with various nucleophiles substitution of the nitroamine group by the nucleophilic reagent took place in all cases.The addition of bromine at the double bond of ketovinylnitroamines took place with difficulty after prolonged heating in benzene or carbon tetrachloride.

A Route from 1,1,1,3-Tetrachloro-3-phenylpropane to Ethynyl Phenyl Ketone Involving Elimination of Hydrogen Chloride and 1,3-Proton Transfer

The treatment of 1,1,1,3-tetrachloro-3-phenylpropane with alkali in ethanol affords ethynyl phenyl ketone and its acetal in good yields.This reaction proceeds through the elimination of hydrogen chloride and an efficient 1,3-proton transfer catalyzed by base.Ethyl cinnamate is obtained in only 2percent yield.