33673-07-3

Basic information

• Product Name: Propanedioic acid, dimethyl ester, ion(1-)
• CAS NO: 33673-07-3
• Molecular Formula: C5H7O4
• Molecular Weight: 131.108
• Mol File: 33673-07-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, dimethyl ester, ion(1-)(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, dimethyl ester, ion(1-)(33673-07-3)
• EPA Substance Registry System: Propanedioic acid, dimethyl ester, ion(1-)(33673-07-3)

Safety Data

• Hazardous Substances Data: 33673-07-3(Hazardous Substances Data)

Downstream Products

• 111170-39-9 2-[3-(2-Benzenesulfonylmethyl-3-methoxy-phenyl)-3-bromo-propyl]-malonic acid dimethyl ester 
• 111170-40-2 2-[3-(2-Benzenesulfonylmethyl-5-methoxy-phenyl)-3-bromo-propyl]-malonic acid dimethyl ester 
• 111170-29-7 2-[3-(2-Benzenesulfonylmethyl-phenyl)-3-bromo-propyl]-malonic acid dimethyl ester 
• 93370-56-0 2-((1S,2S,5S)-2-Iodo-5-methyl-cyclohex-3-enyl)-malonic acid dimethyl ester 
• 93370-55-9 dimethyl (4-iodo-5-methyl-2-cyclohexenyl)malonate 
• 109239-54-5 methyl-3 methoxycarbonyl-2 phenyl-4 pentene-4 oate de methyle 
• 109239-52-3 2-((Z)-2-Phenyl-but-2-enyl)-malonic acid dimethyl ester 
• 111170-31-1 3-(2-Benzenesulfonylmethyl-phenyl)-propionic acid methyl ester 
• 111170-33-3 2-[3-(2-Benzenesulfonylmethyl-phenyl)-propyl]-malonic acid dimethyl ester 
• 102860-23-1 4-(bis(methoxycarbonyl)-methyl)-3-phenylsulfonyl-cyclohexene 
• 102860-24-2 dimethyl ((E)-(phenylsulfonyl)pent-3-en-1-yl)malonate 
• 106501-72-8 dimethyl 2-<2-methoxy-5-(N-benzoylamino)phenyl>malonate 
• 354-33-6 1,1,1,2,2-pentafluoroethane 
• 5464-22-2 tetramethyl ethane-1,1,2,2-tetracarboxylate 

Relevant articles and documents

Intrinsic Reactivities of Some Carbanions in ?-Adduct Forming Reactions

Kinetic and equilibrium data are reported for nucleophilic attack in methanol at unsubstituted ringpositions of 1,3,5-trinitrobenzene, 2,4,6-trinitrotoluene and 1-chloro-2,4,6-trinitrobenzene by carbanions derived from dimethyl malonate, ethyl cyanoacetate and 4-nitro-, 4-cyano- and 2-cyanobenzyl cyanides.The results are used to determine intrinsic reactivities for the carbanions in these ?-adduct forming reactions and are discussed in terms of the electronic and solvent reorganisation occurring during reaction.