1712-36-3

Basic information

• Product Name: Dimethyl-2,3-pentadienedioate
• Synonyms: Dimethyl-2,3-pentadienedioate
• CAS NO: 1712-36-3
• Molecular Formula: C₇H₈O₄
• Molecular Weight: 154.12014
• Mol File: 1712-36-3.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Dimethyl-2,3-pentadienedioate(CAS DataBase Reference)
• NIST Chemistry Reference: Dimethyl-2,3-pentadienedioate(1712-36-3)
• EPA Substance Registry System: Dimethyl-2,3-pentadienedioate(1712-36-3)

Safety Data

• Hazardous Substances Data: 1712-36-3(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 33406-97-2 2,4,6-Tris(diazo)-1,3,5-cyclohexantrione 
• 120461-65-6 dimethyl 3-chloro-2-pentenedioate 
• 186581-53-3 diazomethane 
• 32804-68-5 1,3-allenedicarboxylic acid 
• 1830-54-2 3-oxopentanedioic acid dimethyl ester 

Downstream Products

• 120131-29-5 methyl (4,5,6,7-tetrahydro-5-methoxycarbonyl-4-oxo-2-phenylthieno<2,3-b>pyridin-6-yl)acetate 
• 120131-27-3 dimethyl 3-(3-ethoxycarbonyl-5-phenyl-2-thienylamino)pent-2-enedioate 
• 120131-19-3 (Z)-2-(2-methoxycarbonyl)-1-methoxycarbonylmethylvinylthiobenzoic acid 
• 120131-18-2 (E)-2-(2-methoxycarbonyl)-1-methoxycarbonylmethylvinylthiobenzoic acid 
• 87619-12-3 (E)-3-Phenoxy-pent-2-enedioic acid dimethyl ester 
• 160860-71-9 (1S,2S,4S)-6-Bromo-1-(tert-butyl-diphenyl-silanyloxy)-3-[1-methoxycarbonyl-meth-(E)-ylidene]-5-[(S)-2-(1-methoxy-1-methyl-ethyl)-pyrrolidin-1-yl]-7-oxa-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester 
• 96237-65-9 dimethyl (E)-3-phenoxypent-2-enedioate 
• 100118-53-4 methyl 2-hydroxy-4-methoxy-6-(methoxycarbonylmethyl)benzoate 
• 43071-26-7 methyl 2-hydroxy-6-(methoxycarbonylmethyl)benzoate 
• 64299-72-5 methyl (5-hydroxy-2-methoxycarbonylphenyl)acetate 
• 1051938-46-5 methyl 3-chloro-4-hydroxy-6-(2-methoxy-2-oxoethyl)-2-methylbenzoate 
• 1051938-38-5 methyl 3-chloro-2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzoate 

Relevant articles and documents

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A practical improvement of crystallization-induced asymmetric transformation of allene-1,3-dicarboxylates

Enantiomerically pure allene-1,3-dicarboxylates were easily synthesized by using epimerization-crystallization of dissymmetric allene compounds, which were prepared from acetone-1,3-dicarboxylates and naturally abundant chiral alcohols, that is, (-)- and

A new synthetic method for allene-1,3-dicarboxylates using DMC and a novel tandem cyclization to a pyrrolizidine alkaloid skeleton

A new one-step synthesis of allene-1,3-dicarboxylates from acetone-1,3- dicarboxylates in high yields was developed by the use of DMC as a dehydrating reagent. This process opened a new expeditious mute to a 1- azabicyclo[3.3.0]octane skeleton of pyrrolizidine alkaloids from dimethyl acetone-1,3-dicarboxylate and bis(2-chloroethyl)amine via a Michael addition and a novel tandem cyclization.