6343-00-6

Basic information

• Product Name: (2-hydroxy-3-methoxyphenyl)(2,4,6-trimethoxyphenyl)methanone
• CAS NO: 6343-00-6
• Molecular Formula: C₁₇H₁₈O₆
• Molecular Weight: 318.3212
• Mol File: 6343-00-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 528.6°C at 760 mmHg
• Flash Point: 193.6°C
• Density: 1.215g/cm³
• Vapor Pressure: 8.62E-12mmHg at 25°C
• Refractive Index: 1.559
• CAS DataBase Reference: (2-hydroxy-3-methoxyphenyl)(2,4,6-trimethoxyphenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-hydroxy-3-methoxyphenyl)(2,4,6-trimethoxyphenyl)methanone(6343-00-6)
• EPA Substance Registry System: (2-hydroxy-3-methoxyphenyl)(2,4,6-trimethoxyphenyl)methanone(6343-00-6)

Safety Data

• Hazardous Substances Data: 6343-00-6(Hazardous Substances Data)

Usage

Description

(2-hydroxy-3-methoxyphenyl)(2,4,6-trimethoxyphenyl)methanone is a chemical compound with the molecular formula C17H16O6. It is a yellow crystalline solid that is commonly used in the field of organic synthesis and pharmaceutical research. Its structure contains a combination of hydroxy and methoxy groups attached to phenyl rings, which gives it unique chemical properties and potential applications in various industries.

Uses

Used in Pharmaceutical Research:
(2-hydroxy-3-methoxyphenyl)(2,4,6-trimethoxyphenyl)methanone is used as a pharmaceutical candidate for its potential therapeutic properties. It is being studied for its potential use in the treatment of various diseases and medical conditions.
Used in Organic Synthesis:
(2-hydroxy-3-methoxyphenyl)(2,4,6-trimethoxyphenyl)methanone is used as a reagent in organic chemistry for the synthesis of other organic compounds. Its unique chemical properties make it a valuable component in the creation of new compounds and materials.

Upstream product

• 621-23-8 1,2,3-trimethoxybenzene 
• 7169-06-4 2,3-dimethoxybenzoyl chloride 
• 1521-38-6 2,3-dimethoxybenzoic acid 

Downstream Products

• 53377-61-0 1,3,5-trihydroxy-4-(3-methylbut-2-enyl)-9H-xanthen-9-one 
• 6732-85-0 1,3,5-trihydroxy-9H-xanthen-9-one 
• 33390-41-9 8-deoxygartanin 
• 26486-92-0 6-deoxyisojacareubin 

Relevant articles and documents

Synthesis of 2-hydroxy-3-methylbut-3-enyl substituted coumarins and xanthones as natural products. Application of the Schenck ene reaction of singlet oxygen with ortho-prenylphenol precursors

Application of our original photooxidation-reduction methodology to prenylated dihydroxycoumarin and trihydroxyxanthone compounds led to the corresponding ortho-(2-hydroxy-3-methylbut-3-enyl)phenol derivatives with yields ranging from 8 to 65%. In most of the reported experiments, the oxidation products distribution, after the photooxygenation step, was controlled by the competition between the large group effect and the stabilising phenolic assistance effect. We also showed that ortho-(3-hydroxy-3- methylbut-1-enyl)phenol derivatives could be considered as biogenetic precursors of 2,2-dimethylbenzopyranic structures.