542-05-2
542-05-2
Chemical Structure
3-Oxopentanedioic acid
- CAS No.: 542-05-2
- Formula:C5H6O5
- Molecular Weight:146.10
IUPAC Name: 3-oxopentanedioic acid
InChIKey: OXTNCQMOKLOUAM-UHFFFAOYSA-N
SMILES: O=C(CC(O)=O)CC(O)=O
Biological Activity: 3-Oxopentanedioic acid is a dicarboxylic acid that is easily brominated. 3-Oxopentanedioic acid can be used as an intermediate in organic chemical synthesis[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-Oxopentanedioic acid | 98.50% | 3-Oxopentanedioic acid is a dicarboxylic acid that is easily brominated. 3-Oxopentanedioic acid can be used as an intermediate in organic chemical synthesis. | ||||||||||||||||||||
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3-Oxopentanedioic acid (Standard) | ≥98% | 3-Oxopentanedioic acid (Standard) is the analytical standard of 3-Oxopentanedioic acid (HY-W007752). This product is intended for research and analytical applications. 3-Oxopentanedioic acid is a dicarboxylic acid that is easily brominated. 3-Oxopentanedioic acid can be used as an intermediate in organic chemical synthesis. | ||||||||||||||||||||
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References
- [1]. Sevcík P, et al. Carbon dioxide evolution in a Belousov-Zhabotinsky type oscillating reaction with acetonedicarboxylic acid. J Phys Chem A. 2007 Oct 11;111(40):10050-4. [Content Brief]
- [2]. Abignente E, et al. Research on heterocyclic compounds. XIII. Synthesis of 4, 5‐dihydro‐5‐oxo‐3‐isoxazoleacetic acid and related compounds. Journal of heterocyclic chemistry, 1983, 20(6): 1597-1599.
- [3]. Liu ZQ, et al. Formation of brominated trihalomethanes during chlorination or ozonation of natural organic matter extracts and model compounds in saline water. Water Res. 2018 Oct 15;143:492-502. [Content Brief]
