896-90-2

Basic information

• Product Name: Propanedioic acid, (3,4-dimethoxyphenyl)-, diethyl ester
• CAS NO: 896-90-2
• Molecular Formula: C15H20O6
• Molecular Weight: 296.32
• Mol File: 896-90-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, (3,4-dimethoxyphenyl)-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, (3,4-dimethoxyphenyl)-, diethyl ester(896-90-2)
• EPA Substance Registry System: Propanedioic acid, (3,4-dimethoxyphenyl)-, diethyl ester(896-90-2)

Safety Data

• Hazardous Substances Data: 896-90-2(Hazardous Substances Data)

Upstream product

• 18066-68-7 ethyl 3,4-dimethoxyphenylacetate 
• 105-58-8 Diethyl carbonate 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 623-49-4 ethyl cyanoformate 
• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 121324-66-1 2-(3,4-Dimethoxy-phenyl)-N,N'-dipropyl-malonamide 
• 926008-52-8 5-(3,4-dimethoxyphenyl)pyrimidine-4,6-diol 
• 799-88-2 1,1-Di-ethoxycarbonyl-3-(3,4-dimethoxyphenyl)-cyclobutan 
• 810-53-7 2-(3,4-Dimethoxy-phenyl)-1,3-propane-diyl di-p-toluene sulphonate 
• 121324-78-5 2-(3,4-Dimethoxy-phenyl)-N,N'-bis-[2-(3,4-dimethoxy-phenyl)-ethyl]-propane-1,3-diamine 
• 121324-77-4 2-(3,4-Dimethoxy-phenyl)-N,N'-diphenethyl-propane-1,3-diamine 
• 121324-76-3 N,N'-Dibenzyl-2-(3,4-dimethoxy-phenyl)-propane-1,3-diamine 
• 121324-75-2 N,N'-Dicyclohexyl-2-(3,4-dimethoxy-phenyl)-propane-1,3-diamine 
• 121324-74-1 N,N'-Di-n-butyl-2-(3,4-dimethoxy-phenyl)-1,3-propane-diamine 
• 121324-73-0 2-(3,4-Dimethoxy-phenyl)-N,N'-dipropyl-propane-1,3-diamine 
• 121324-72-9 2-(3,4-Dimethoxy-phenyl)-N,N'-diethyl-propane-1,3-diamine 
• 926008-72-2 {4-[6-chloro-5-(3,4-dimethoxyphenyl)pyrimidin-4-ylethynyl]phenyl}dimethylamine 
• 146533-38-2 4,6-dichloro-5-(3,4-dimethoxyphenyl)pyrimidine 
• 717-51-1 2-(3,4-dimethoxy-phenyl)-1,3-propane-diol 

Relevant articles and documents

Enzymatic desymmetrization of prochiral 2-substituted-1,3-diamines: Preparation of valuable nitrogenated compounds

A wide range of prochiral 1, 3-diamines were first efficiently synthesized and subsequently desymmetrized by using lipase from Pseudomonas cepacia as catalyst and diallyl carbonate as alkoxycarbonylating agent. In all cases, the amino carbamates of R-configuration were recovered. Final selective cleavage of the N-allyloxycarbonyl moiety was carried out under mild reaction conditions, which demonstrates the high versatility and potential of this chemoenzymatic route as a source of intermediates in the synthesis of related optically active nitrogenated derivatives.

Synthesis of some 2-(3,4-dimethoxy-phenyl)-1,3-propanediamines as potential dopaminergic agents

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