1621-91-6
Chemical Structure
Pyrazole-3-carboxylic acid
- CAS No.: 1621-91-6
- Formula:C4H4N2O2
- Molecular Weight:112.09
IUPAC Name: 1H-pyrazole-3-carboxylic acid
InChIKey: KOPFEFZSAMLEHK-UHFFFAOYSA-N
SMILES: O=C(C1=NNC=C1)O
Biological Activity: Pyrazole-3-carboxylic acid is an alternative anchoring group to carboxylic acid in phthalocyanine dyes. Pyrazole-3-carboxylic acid shows flexible coordination modes when coordinates with metal ions. Pyrazole-3-carboxylic acid can chelate to metal ions and form very stable complexes through its N and O atoms. Pyrazole-3-carboxylic acid can be used to synthesize derivatives that possess antibacterial, anti-inflammatory, ulcerogenic liability and antiproliferative activities[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Pyrazole-3-carboxylic acid | 99.97% | Pyrazole-3-carboxylic acid is an alternative anchoring group to carboxylic acid in phthalocyanine dyes. Pyrazole-3-carboxylic acid shows flexible coordination modes when coordinates with metal ions. Pyrazole-3-carboxylic acid can chelate to metal ions and form very stable complexes through its N and O atoms. Pyrazole-3-carboxylic acid can be used to synthesize derivatives that possess antibacterial, anti-inflammatory, ulcerogenic liability and antiproliferative activities. | ||||||||||||||||||||
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References
- [1]. Burak Yıldız, et al., (2018) Pyrazole-3-carboxylic acid as a new anchoring group for phthalocyanine-sensitized solar cells, Solar Energy, Volume 174, Pages 527-536, ISSN 0038-092X.
- [2]. Abdel-Hafez, el-S. M., et al., (2009). Design, synthesis and biological investigation of certain pyrazole-3-carboxylic acid derivatives as novel carriers for nitric oxide. Bioorganic & medicinal chemistry, 17(11), 3829–3837. [Content Brief]
- [3]. Kasımoğulları, R., et al., Design, synthesis, characterization, and antiproliferative activity of novel pyrazole-3-carboxylic acid derivatives. Monatsh Chem 146, 1743–1749 (2015).
