6399-14-0

Basic information

• Product Name: 4α-(3,4-dimethoxyphenyl)-2α,3β-dimethyl-6,7-dimethoxy-1-tetralone
• CAS NO: 6399-14-0
• Molecular Weight: 370.445
• Mol File: 6399-14-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 4α-(3,4-dimethoxyphenyl)-2α,3β-dimethyl-6,7-dimethoxy-1-tetralone(CAS DataBase Reference)
• NIST Chemistry Reference: 4α-(3,4-dimethoxyphenyl)-2α,3β-dimethyl-6,7-dimethoxy-1-tetralone(6399-14-0)
• EPA Substance Registry System: 4α-(3,4-dimethoxyphenyl)-2α,3β-dimethyl-6,7-dimethoxy-1-tetralone(6399-14-0)

Safety Data

• Hazardous Substances Data: 6399-14-0(Hazardous Substances Data)

Upstream product

• 98333-30-3 5,5-bis-(3,4-dimethoxy-phenyl)-3,4-dimethyl-dihydro-furan-2-one 
• 74084-26-7 3,3',4,4'-tetramethoxybenzhydrole 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 4131-03-7 bis(3,4-dimethoxyphenyl)methanone 
• 521-54-0 (±)-galbulin 
• 3569-00-4 (+/-)-trans-4-(3,4-dimethoxyphenyl)-3,4-dihydro-6,7-dimethoxy-2,3-dimethylnaphthalene 
• 776-99-8 3,4-dimethoxyphenylacetone 

Downstream Products

• 521-54-0 1β-(3,4-dimethoxyphenyl)-2β,3α-dimethyl-6,7-dimethoxytetralin 
• 521-54-0 (±)-galbulin 

Relevant articles and documents

Aryltetralols from Holostylis reniformis and syntheses of lignan analogous

Abstract Two new lignans, an aryltetralol and its methyl ether analogous, were isolated from Holostylis reniformis (Aristolochiaceae) together with futokadsurin C and (-)-8′-epi-aristoligone. The latter was also obtained as an enantiomeric mixture by synt

Collective synthesis of several 2,7′-cyclolignans and their correlation by chemical transformations

Collective synthesis of anti-malarial 2,7′-cyclolignans has been stereoselectively achieved employing (±)-cyclogalgravin (2) as a linchpin through a series of functional group conversions, including redox reactions. Interestingly, 2 can be correlated with

New Reagent System containing CrO3 and Syntheses of Neo-lignans

Oxidations of 1-arylprop-1-enes by the new reagent systems, CrO3-HBF4-MeCN or CrO3-HClO4-MeCN gave the 4-aryltetralones (1a) and (1c), and the tetrahydrofuran (3) which are precursor molecules for aryltetrahydronaphthalene and tetrahydrofuran neo-lignans.