7507-98-4

Basic information

• Product Name: 1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone
• Synonyms: 2-Hydroxy-3,4,6-trimethoxyacetophenone
• CAS NO: 7507-98-4
• Molecular Formula: C₁₁H₁₄O₅
• Molecular Weight: 226.2259
• Mol File: 7507-98-4.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 365.3°C at 760 mmHg
• Flash Point: 140.1°C
• Density: 1.181g/cm³
• Vapor Pressure: 7.54E-06mmHg at 25°C
• Refractive Index: 1.52
• CAS DataBase Reference: 1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone(7507-98-4)
• EPA Substance Registry System: 1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone(7507-98-4)

Safety Data

• Hazardous Substances Data: 7507-98-4(Hazardous Substances Data)

Usage

General Description

1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone is a chemical compound with the molecular formula C11H14O5. It is a yellow crystalline solid that is found naturally in various plants and fruits. It is also known by the name "galanganal" and is commonly used in the food and beverage industry as a flavoring agent. It has a sweet, spicy, and slightly floral aroma and is often used in the production of perfumes and cosmetics. Additionally, it has been studied for its potential health benefits, including antioxidant and anti-inflammatory properties. 1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone has potential applications in the pharmaceutical industry and is currently being researched for its medicinal properties.

Upstream product

• 123316-62-1 5,7,8,2',4'-pentamethoxyflavone 
• 7499-99-2 1-(2,4-dihydroxy-3,6-dimethoxy)phenylethanone 
• 74-88-4 methyl iodide 
• 123316-61-0 2-(2,4-dimethoxyphenyl)-5-hydroxy-7,8-dimethoxy-4H-chromen-4-one 
• 5333-45-9 1,2,3,5-tetramethoxybenzene 
• 15233-65-5 2,6-dimethoxy-1,4-hydroquinone 
• 642-71-7 3,4,5-trimethoxyphenol 
• 6953-31-7 2'-acetoxy-3',4',5'-trimethoxyacetophenone 
• 67-64-1 acetone 
• 77-78-1 dimethyl sulfate 
• 71-43-2 benzene 
• 75-36-5 acetyl chloride 
• 7446-70-0 aluminium trichloride 
• 7508-05-6 1-(2,3,4,6-tetramethoxyphenyl)ethanone 

Downstream Products

• 111797-34-3 2'-hydroxy-3',4',6'-trimethoxy-4-methoxymethoxy-trans-chalcone 
• 6953-31-7 2'-acetoxy-3',4',5'-trimethoxyacetophenone 
• 91856-17-6 (E)-1-(2-hydroxy-3,4,6- trimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one 
• 23050-38-6 5,7,8-trimethoxy-2-phenyl-chromen-4-one 
• 23806-72-6 2'-hydroxy-2,3,3',4',6'-pentamethoxy-trans-chalcone 
• 110561-87-0 2'-Hydroxy-3',4',6',2-tetramethoxy-4-benzyloxychalkone 
• 76011-61-5 2-(3'-benzyloxy-4',5'-dimethoxy)benzoyloxy-3,4,6-trimethoxyacetophenone 
• 111670-52-1 4-benzyloxy-2'-hydroxy-3',4',6',3,5-pentamethoxychalkone 
• 101909-55-1 2-(2',4'-diisopropyloxybenzoyloxy)-3,4,6-trimethoxyacetophenone 
• 101923-85-7 2-(2',5'-diisopropyloxybenzoyloxy)-3,4,6-trimethoxyacetophenone 
• 110561-90-5 2-(4'-Benzyloxy-2'-methoxy)benzoyloxy-3,4,6-trimethoxyacetophenone 
• 103451-02-1 2'-hydroxy-2,4-diisopropyloxy-3',4',6',5-tetramethoxychalcone 
• 7508-05-6 1-(2,3,4,6-tetramethoxyphenyl)ethanone 
• 111670-55-4 2'-hydroxy-3-benzyloxy-3',4',6',4-tetramethoxychalkone 

Relevant articles and documents

A facile 2: H -chromene dimerization through an ortho -quinone methide intermediate catalyzed by a sulfonyl derived MIL-101 MOF

A MIL-101-SO3H MOF was synthesized using commercially available materials. The as-synthesized MIL-101-SO3H was characterized by SEM, XRD, FTIR, BET and TGA. An efficient and diastereoselective homo-dimerization of 2H-chromenes cataly

Iron-catalyzed rearrangements and cycloaddition reactions of 2h-chromenes

Iron(III) salts catalyze the tandem rearrangement/hetero-Diels-Alder reaction of 2H-chromenes to yield tetrahydrochromeno heterocycles. The process can occur as a homodimerization and cycloaddition process using electron-rich dienophiles. Deuterium labeli

Acid catalyzed stereoselective rearrangement and dimerization of flavenes: synthesis of dependensin

Appropriately substituted flavenes undergo stereoselective rearrangement and dimerization when treated with methanolic hydrochloric acid to give benzopyranobenzopyrans. A rationale for the rearrangement is proposed. This synthetic methodology has been used for a high yield synthesis of the natural product dependensin.