94762-80-8

Basic information

• Product Name: 2,3-bis(3,4-dimethoxyphenyl)butane-2,3-diol
• Synonyms: 2,3-bis(3,4-dimethoxyphenyl)butane-2,3-diol
• CAS NO: 94762-80-8
• Molecular Weight: 362.423
• Mol File: 94762-80-8.mol

Chemical Properties

• CAS DataBase Reference: 2,3-bis(3,4-dimethoxyphenyl)butane-2,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-bis(3,4-dimethoxyphenyl)butane-2,3-diol(94762-80-8)
• EPA Substance Registry System: 2,3-bis(3,4-dimethoxyphenyl)butane-2,3-diol(94762-80-8)

Safety Data

• Hazardous Substances Data: 94762-80-8(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 22675-96-3 2-methoxyphenoxy-3',4'-dimethoxyacetophenone 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 73786-26-2 (2S,3aR)-2-(3,4-Dimethoxy-phenyl)-2-[1-(3,4-dimethoxy-phenyl)-vinyl]-hexahydro-pyrrolo[1,2-b]isoxazole 
• 73786-26-2 isoxazolidine 
• 73786-27-3 (1R,5S,7S,8R)-8-Bromo-7,8-bis-(3,4-dimethoxy-phenyl)-10-oxa-1-azonia-tricyclo[5.2.1.0^1,5]decane; bromide 
• 73786-28-4 (1aR,2aR,6aR)-1a,6a-Bis-(3,4-dimethoxy-phenyl)-octahydro-1-oxa-5a-aza-cyclopropa[f]indene 
• 74170-42-6 (R)-2,3-Bis-(3,4-dimethoxy-phenyl)-1-(R)-pyrrolidin-2-yl-but-3-en-2-ol 
• 5385-61-5 4,4'-(ethene-1,1-diyl)bis(1,2-dimethoxybenzene) 
• 26503-67-3 (+/-)-6,7-di(3,4-dimethoxyphenyl)-1,2,3,5,8,8a-hexahydro-indolizine 
• 73786-25-1 2,3-bis(3,4-dimethoxyphenyl)-1,3-butadiene 

Relevant articles and documents

SYNTHESIS OF dl-SEPTICINE

Cyloaddition reaction of 1-pyrroline 1-oxide with 2,3-bis(3,4-dimethoxyphenyl)butadiene proceeded regioselectively to give two stereoisomeric isoxazolidine derivatives, one of which was converted into septicine by three-step reactions.

Electro-reductive Fragmentation of Oxidized Lignin Models

Lignin provides a potential sustainable source for production of electron-rich aromatic compounds. Recently, electrochemical lignin degradation via an oxidation/reduction sequence under mild conditions has garnered much attention within the lignin community, as electrochemistry simplifies redox reactions and offers an electron source/sink for synthesis without using stoichiometric oxidants or reductants. This paper describes a fundamental approach for the electrochemical fragmentation of the primary connection in native lignin, β-O-4. Potential-controlled electrolysis enables selective reduction and provides fragmentation products and/or coupling products in isolated yields of 59-92%.