835-25-6

Basic information

• Product Name: 1-(2,4,6-Trimethoxyphenyl)propan-2-one
• Synonyms: 1-(2,4,6-Trimethoxyphenyl)propan-2-one;1-(2,4,6-Trimethoxyphenyl)-2-propanone
• CAS NO: 835-25-6
• Molecular Formula: C₁₂H₁₆O₄
• Molecular Weight: 224.25304
• Mol File: 835-25-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 87-88 °C
• Boiling Point: 328.2±37.0 °C(Predicted)
• Appearance: /
• Density: 1.078±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-(2,4,6-Trimethoxyphenyl)propan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4,6-Trimethoxyphenyl)propan-2-one(835-25-6)
• EPA Substance Registry System: 1-(2,4,6-Trimethoxyphenyl)propan-2-one(835-25-6)

Safety Data

• Hazardous Substances Data: 835-25-6(Hazardous Substances Data)

Usage

Chemical class

Phenylpropanoids Tropinone belongs to the class of organic compounds known as phenylpropanoids, which are derived from phenylalanine and have a propyl side chain.

Structure

Ketone derivative Tropinone is a ketone derivative, which means it contains a carbonyl group (C=O) bonded to two carbon atoms.

Substituents

Three methoxy groups Tropinone has three methoxy groups (-OCH3) attached to the phenyl ring, which gives it unique properties and chemical reactivity.

Pharmacological activities

Tropinone is known to have various pharmacological activities, making it a subject of interest for medicinal applications.

Medicinal applications

Tropinone has been studied for its potential use in the development of new drugs and therapies.

Building block

Tropinone is used as a building block for the synthesis of other organic compounds in the pharmaceutical and chemical industries.

Applications

Tropinone has important applications in the field of chemistry and medicinal research, making it a valuable compound for further study and development.

Synonyms

Tropinone is also known as 1-(2,4,6-Trimethoxyphenyl)propan-2-one, which highlights its chemical structure and functional groups.

Upstream product

• 78904-45-7 1-(2,4,6-trimethoxyphenyl)-2-nitro-1-propene 
• 835-24-5 1-(2,4,6-trimethoxyphenyl)propan-2-ol 
• 2215-80-7 <4-Hydroxy-2,6-dimethoxy-phenyl>-aceton 
• 77-78-1 dimethyl sulfate 
• 5273-96-1 (E)-1,3,5-trimethoxy-2-(prop-1-en-1-yl)benzene 
• 91353-27-4 4-Hydroxy-2,6-dimethoxy-phenylisopropanol 
• 5030-76-2 1-(1-Acetoxy-acetonyl)-4-acetoxy-2,6-dimethoxy-benzol 
• 621-23-8 1,2,3-trimethoxybenzene 
• 67-64-1 acetone 

Downstream Products

• 835-24-5 1-(2,4,6-trimethoxyphenyl)propan-2-ol 
• 2215-97-6 2-n-propyl-1,3,5-trimethoxybenzene 
• 134040-38-3 2,4,6-trimethoxy-β-methyl-β-nitrostyrene 

Relevant articles and documents

Philicity of Acetonyl and Benzoyl Radicals: A Comparative Experimental and Computational Study

In this work, the reactivities of acetonyl and benzoyl radicals in aromatic substitution and addition reactions have been compared in an experimental and computational study. The results show that acetonyl is more electrophilic than benzoyl, which is rath