213267-13-1

Basic information

• Product Name: 1-(3,4-dimethoxyphenyl)-2,2-dimethylpropan-1-ol
• Synonyms: 1-(3,4-dimethoxyphenyl)-2,2-dimethylpropan-1-ol
• CAS NO: 213267-13-1
• Molecular Weight: 224.3
• Mol File: 213267-13-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(3,4-dimethoxyphenyl)-2,2-dimethylpropan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-dimethoxyphenyl)-2,2-dimethylpropan-1-ol(213267-13-1)
• EPA Substance Registry System: 1-(3,4-dimethoxyphenyl)-2,2-dimethylpropan-1-ol(213267-13-1)

Safety Data

• Hazardous Substances Data: 213267-13-1(Hazardous Substances Data)

Upstream product

• 30314-46-6 1-(3,4-dimethoxyphenyl)-2,2-dimethylpropan-1-one 
• 594-19-4 tert.-butyl lithium 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 30314-46-6 1-(3,4-dimethoxyphenyl)-2,2-dimethylpropan-1-one 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 563-80-4 3-methyl-butan-2-one 
• 120-80-9 benzene-1,2-diol 

Relevant articles and documents

Br?nsted Acid Catalyzed Tandem Defunctionalization of Biorenewable Ferulic acid and Derivates into Bio-Catechol

An efficient conversion of biorenewable ferulic acid into bio-catechol has been developed. The transformation comprises two consecutive defunctionalizations of the substrate, that is, C?O (demethylation) and C?C (de-2-carboxyvinylation) bond cleavage, occurring in one step. The process only requires heating of ferulic acid with HCl (or H2SO4) as catalyst in pressurized hot water (250 °C, 50 bar N2). The versatility is shown on a variety of other (biorenewable) substrates yielding up to 84 % di- (catechol, resorcinol, hydroquinone) and trihydroxybenzenes (pyrogallol, hydroxyquinol), in most cases just requiring simple extraction as work-up.