39701-13-8

Basic information

• Product Name: 1-(2,4,6-trimethoxy-3-methylphenyl)ethan-1-one
• Synonyms: 1-(2,4,6-trimethoxy-3-methylphenyl)ethan-1-one
• CAS NO: 39701-13-8
• Molecular Weight: 224.257
• Mol File: 39701-13-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(2,4,6-trimethoxy-3-methylphenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4,6-trimethoxy-3-methylphenyl)ethan-1-one(39701-13-8)
• EPA Substance Registry System: 1-(2,4,6-trimethoxy-3-methylphenyl)ethan-1-one(39701-13-8)

Safety Data

• Hazardous Substances Data: 39701-13-8(Hazardous Substances Data)

Upstream product

• 52200-61-0 2,4-dihydroxy-6-methoxy-5-methyl-acetophenone 
• 77-78-1 dimethyl sulfate 
• 23121-32-6 1-(2-hydroxy-4,6-dimethoxy-3-methyl-phenyl)-ethanone 
• 2657-28-5 2,4,6-trihydroxy-3-methyl-acetophenon 
• 74-88-4 methyl iodide 
• 14107-97-2 2,4,6-trimethoxytoluene 
• 75-36-5 acetyl chloride 
• 61040-78-6 2,4,6-trimethoxybenzyl alcohol 
• 830-79-5 2,4,6-trimethoxybenzaldehyde 
• 102749-22-4 1-(4,6-bis-benzyloxy-2-methoxy-3-methyl-phenyl)-ethanone 

Downstream Products

• 106929-57-1 3-methyl-2-hydroxy-4,6-bis(methoxymethoxy)acetophenone 
• 916917-16-3 8-methyl-5,7,4'-tris(methoxymethoxy)flavanone 
• 916917-28-7 (+/-)-8-Methylnaringenin 
• 2657-28-5 2,4,6-trihydroxy-3-methyl-acetophenon 

Relevant articles and documents

STRUCTURE DETERMINATION OF MELANERVIN, THE FIRST NATURALLY OCCURING FLAVONOID OF THE TRIPHENYLMETHANE FAMILY

From the flowers of Melaleuca quinquenervia (Myrtaceae) besides the flavonones strobopinin and kryptostrobin a new 8-aryl-flavonone has been isolated and shown to be (2,4-dihydroxy-6-methoxy)tolyl-3-(5,7-dihydroxy-6-methyl)flavanonyl-8-phenylmethane, mainly by degradation, MS, 1H- and 13C-NMR-spectroscopy.The new flavanone represents the first naturally occuring triphenylmethane compound.

Efficient synthesis of rottlerin and its two subunits

Rottlerin, a natural product isolated from Mallotus philippensis, is associated with a range of biological activities. Its chemical structure is featured by two different substituted phloroglucinol units linked by a methylene group. In this study, we accomplished a total synthesis of rottlerin using phenol-aldehyde condensation as the key reaction. By our method, gram-scale preparation of the two structural subunits was achieved, and rottlerin was obtained in a longest eight linear step with 20% overall yield. Our study provides a practical solution for obtaining the sample of rottlerin in an efficient way.

Synthesis of aurentiacin

Aurentiacin 7 has been isolated from Pityrogramma triangularis var. pallida and synthesised from phloroacetophenone 1 in several steps. All the new products have been characterised on the basis of spectral data and micro analysis.