| Weight | 102.089 g/mol |
|---|---|
| Formula | C4H6O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
2-oxobutanoic acid (600-18-0)
2-ketobutyrate · 2-oxobutanoate · alpha-ketobutyric acid
Score:
#1179 in Biochemistry
,
#3724 in Chemistry
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- Sigma-Aldrich - 2-oxobutanoic acid43.20 - 520.00 USD
- Fisher Scientific - Search for 2-oxobutanoic acid
- TCI - 2-oxobutanoic acid152.00 USD
- Three-dimensional structure of 2-amino-3-ketobutyrate CoA ligase from Escherichia coli complexed with a PLP-substrate intermediate: inferred reaction mechanism. (Biochemistry, 2001)
- Diastereo- and enantio-selective reduction of 2-methyl-3-oxobutanoate by Bakers' yeast (Tetrahedron Letters, 1986)
- Stereochemical control in microbial reduction. 9. Diastereoselective reduction of 2-alkyl-3-oxobutanoate with bakers' yeast. (Bulletin of the Chemical Society of Japan, 1989)
- UV filter compounds in human lenses : The origin of 4-(2-amino-3-hydroxyphenyl)-4-oxobutanoic acid O--D-glucoside (Investigative Ophthalmology & Visual Science, 1999)
- Highly stereoselective asymmetric hydrogenation of 2-benzamidomethyl-3-oxobutanoate catalysed by cationic binapruthenium(II) complexes (Journal of The Chemical Society, Chemical Communications, 1991)
- Phytotoxicity of Acetohydroxyacid Synthase Inhibitors Is Not Due to Accumulation of 2-Ketobutyrate and/or 2-Aminobutyrate (Plant Physiology, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-ketobutyrate
- 2-oxobutanoate
- alpha-ketobutyric acid
- 2-ketobutyric acid
- 2-oxobutyrate
- alpha-ketobutyric acid, sodium salt
- alpha-oxobutyric acid
-
SMILESCCC(=O)C(=O)O
-
InChIKeyTYEYBOSBBBHJIV-UHFFFAOYSA-N
- Pubchem - 2-oxobutanoic acid
- Wikipedia - -ketobutyric acid
-Ketobutyric acid is a product of the lysis of cystathionine. It is also one of the degradation products of threonine, produced by the catabolism of the amino acid by threonine dehydratase. It is also produced by the degradation of homocysteine and the metabolism of methionine.
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2-oxobutanoic acid
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