3-Methyl-2-Oxo-Butanoic Acid 2-氧代-3-甲基丁酸
CAS 759-05-7 MFCD00040427
化学结构图
SMILES:
化学属性
| Mol. Formula | C5H8O3 |
|---|---|
| Mol. Weight | 116.12 |
| Melting Point | 31.5°C |
| Boiling Point | 170.2°C at 760 mmHg |
| Flash Point | 71.0±15.2°C |
别名和识别编码
| Chemical Name | 3-Methyl-2-Oxo-Butanoic Acid |
|---|---|
| Chemical Name Translation | 2-氧代-3-甲基丁酸 |
| LabNetwork Molecule ID | LN00190076 |
| CAS Number | 759-05-7 |
| Synonym | 3-Methyl-2-oxobutanoic acid {LY} 3-Methyl-2-oxobutanoic acid {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 3-Methyl-2-oxobutanoic acid {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 3-Methy |
| Canonical SMILES | CC(C)C(C(O)=O)=O |
| MDL Number | MFCD00040427 |
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相关文献及参考
- [2]. Schauder P, et al. Oral administration of alpha-ketoisovaleric acid or valine in humans: blood kinetics and biochemical effects. J Lab Clin Med. 1984 Apr;103(4):597-605.
- [3]. Coitinho AS, et al. Pharmacological evidence that alpha-ketoisovaleric acid induces convulsions through GABAergic and glutamatergic mechanisms in rats. Brain Res. 2001 Mar 9;894(1):68-73.
- [1]. MAAS WK, et al. alpha-Ketoisovaleric acid, a precursor of pantothenic acid in Escherichia coli. J Bacteriol. 1953 Apr;65(4):388-93.
- [1]. MAAS WK, et al. alpha-Ketoisovaleric acid, a precursor of pantothenic acid in Escherichia coli. J Bacteriol. 1953 Apr;65(4):388-93.
- [2]. Schauder P, et al. Oral administration of alpha-ketoisovaleric acid or valine in humans: blood kinetics and biochemical effects. J Lab Clin Med. 1984 Apr;103(4):597-605.
- [3]. Coitinho AS, et al. Pharmacological evidence that alpha-ketoisovaleric acid induces convulsions through GABAergic and glutamate
