dimethyl 2-oxobutanedioate

Base Information

  • Chemical Name: dimethyl 2-oxobutanedioate
  • CAS No.: 25007-54-9

Factory Sells Best Quality dimethyl 2-oxobutanedioate 25007-54-9 with ISO standards

  • Molecular Formula: C6H8 O5
  • Molecular Weight: 160.127
  • Vapor Pressure: 0.128mmHg at 25°C 
  • Melting Point: 85 °C 
  • Boiling Point: 218.1°Cat760mmHg 
  • PKA: 7.92±0.46(Predicted) 
  • Flash Point: 88.5°C 
  • PSA: 69.67000 
  • Density: 1.216g/cm3 
  • LogP: -0.70840 

dimethyl 2-oxobutanedioate(Cas 25007-54-9) Usage

General Description

Dimethyl 2-oxobutanedioate is a chemical compound with the molecular formula C6H8O5. It is also known as dimethyl pyruvate, and it is an ester of pyruvic acid. dimethyl 2-oxobutanedioate is often used as a reagent in organic synthesis, specifically in the formation of various pharmaceuticals and other organic compounds. Dimethyl 2-oxobutanedioate is a colorless, pleasant-smelling liquid with a melting point of -57°C and a boiling point of 119-120°C. It is soluble in water and ethanol, and it is commonly used as a precursor in the synthesis of pyruvate-derived compounds. Additionally, it is known to have antimicrobial and antioxidant properties, making it potentially useful in various industrial and medicinal applications.

InChI:InChI=1/C6H8O5/c1-10-5(8)3-4(7)6(9)11-2/h3H2,1-2H3

25007-54-9 Relevant articles

Thermal rearrangements of tetrahydroimidazo[1,5-b]isoxazole-2,3-dicarboxylates. Synthesis of 3H-imidazol-1-ium ylides and their silver derivatives

Co?kun, Necdet,?etin, Meliha

experimental part, p. 2053 - 2060 (2010/04/26)

Isoxazolines 2 from the cycloaddition of...

FT-IR kinetic and product study of the OH radical and Cl-atom - Initiated oxidation of dibasic esters

Cavalli, Fabrizia,Barnes, Ian,Becker, Karl Heinz

, p. 431 - 439 (2007/10/03)

Using a relative kinetic technique, rate...

Synthesis of β-Dicarbonyl Compounds via the Conjugate Addition of Benzaldoximate Anion to α,β-Acetylenic Carbonyl Compounds

Gomez, Virginia,Perez-Medrano, Arturo,Muchowski, Joseph M.

, p. 1219 - 1221 (2007/10/02)

-

REACTION OF ETHYL 2-AMINO-4,6-O-BENZYLIDENE-2-DEOXY-D-GLUCONATE WITH ACETYLENIC ESTERS

Miquel, Luis M. Vazquez de,Blazquez, Jose A. Serrano,Barros, Fernando J. Garcia,Guillen, Manuel Gomez

, p. 81 - 90 (2007/10/02)

Ethyl 2-amino-4,6-O-benzylidene-2-deoxy-...

25007-54-9 Process route

syn-benzaldehyde oxime
932-90-1,622-31-1,140461-24-1,140461-25-2,622-32-2

syn-benzaldehyde oxime

dimethyl acetylenedicarboxylate
762-42-5

dimethyl acetylenedicarboxylate

Dimethyl 2-oxosuccinate
25007-54-9

Dimethyl 2-oxosuccinate

benzonitrile
100-47-0

benzonitrile

Conditions
Conditions Yield
With sodium hydride; In tetrahydrofuran; 1.) r.t., 0.5 h, 2.) -20 deg C, 2 h;
57%
44%
methyl (4R,5R)-5-(1,3-O-benzylidene-D-erythro-glycerol-1-yl)-4-(ethoxycarbonyl)-2-(methoxycarbonyl)oxazolidin-2-yl acetate
91288-16-3

methyl (4R,5R)-5-(1,3-O-benzylidene-D-erythro-glycerol-1-yl)-4-(ethoxycarbonyl)-2-(methoxycarbonyl)oxazolidin-2-yl acetate

D-glucosaminic acid
3646-68-2

D-glucosaminic acid

Dimethyl 2-oxosuccinate
25007-54-9

Dimethyl 2-oxosuccinate

benzaldehyde
100-52-7

benzaldehyde

Conditions
Conditions Yield
With hydrogenchloride; at 100 ℃; for 2h;
0.43 g
With hydrogenchloride; ethanol; Yield given. Multistep reaction; 1.) 100 deg C, 2 h;
0.43 g

25007-54-9 Upstream products

  • 91288-16-3
    91288-16-3

    methyl (4R,5R)-5-(1,3-O-benzylidene-D-erythro-glycerol-1-yl)-4-(ethoxycarbonyl)-2-(methoxycarbonyl)oxazolidin-2-yl acetate

  • 932-90-1
    932-90-1

    syn-benzaldehyde oxime

  • 762-42-5
    762-42-5

    dimethyl acetylenedicarboxylate

  • 106-65-0
    106-65-0

    Dimethyl succinate

25007-54-9 Downstream products

  • 22158-22-1
    22158-22-1

    phenylhydrazono-succinic acid dimethyl ester

  • 86625-25-4
    86625-25-4

    3-methoxycarbonyl-5-pyrazolinone

  • 7101-82-8
    7101-82-8

    dimethyl 2-((2-methoxyphenyl)amino)but-2-enedioate

  • 93729-64-7
    93729-64-7

    4,5-dioxo-1,2-diphenyl-pyrrolidine-3-carboxylic acid methyl ester

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