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
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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)
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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
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932-90-1,622-31-1,140461-24-1,140461-25-2,622-32-2
syn-benzaldehyde oxime
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762-42-5
dimethyl acetylenedicarboxylate
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25007-54-9
Dimethyl 2-oxosuccinate
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100-47-0
benzonitrile
| Conditions | Yield |
|---|---|
|
With
sodium hydride;
In
tetrahydrofuran;
1.) r.t., 0.5 h, 2.) -20 deg C, 2 h;
|
57%
44% |
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91288-16-3
methyl (4R,5R)-5-(1,3-O-benzylidene-D-erythro-glycerol-1-yl)-4-(ethoxycarbonyl)-2-(methoxycarbonyl)oxazolidin-2-yl acetate
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3646-68-2
D-glucosaminic acid
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25007-54-9
Dimethyl 2-oxosuccinate
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100-52-7
benzaldehyde
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
at 100 ℃;
for 2h;
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0.43 g
|
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With
hydrogenchloride; ethanol;
Yield given. Multistep reaction;
1.) 100 deg C, 2 h;
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0.43 g
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25007-54-9 Upstream products
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91288-16-3
methyl (4R,5R)-5-(1,3-O-benzylidene-D-erythro-glycerol-1-yl)-4-(ethoxycarbonyl)-2-(methoxycarbonyl)oxazolidin-2-yl acetate
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932-90-1
syn-benzaldehyde oxime
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762-42-5
dimethyl acetylenedicarboxylate
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106-65-0
Dimethyl succinate
25007-54-9 Downstream products
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22158-22-1
phenylhydrazono-succinic acid dimethyl ester
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86625-25-4
3-methoxycarbonyl-5-pyrazolinone
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7101-82-8
dimethyl 2-((2-methoxyphenyl)amino)but-2-enedioate
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93729-64-7
4,5-dioxo-1,2-diphenyl-pyrrolidine-3-carboxylic acid methyl ester