303180-11-2
Chemical Structure
1H-pyrazole-3,5-dicarboxylic acid hydrate
Synonym(s): Pyrazole-3,5-dicarboxylic acid monohydrate
- CAS No.: 303180-11-2
- Formula:C5H6N2O5
- Molecular Weight:174.11
IUPAC Name: 1H-pyrazole-3,5-dicarboxylic acid hydrate
InChIKey: GLINCONFUZIMCN-UHFFFAOYSA-N
SMILES: O=C(O)C1=NNC(=C1)C(=O)O.O
Biological Activity: 1H-pyrazole-3,5-dicarboxylic acid hydrate (Pyrazole-3,5-dicarboxylic acid monohydrate) serves as a precursor for the synthesis of 26-membered diazatetraester crown ethers and 39-membered triazahexaester crown ethers containing pyrazole units. 1H-pyrazole-3,5-dicarboxylic acid hydrate acts as a V-type heterocyclic polycarboxylic acid bridging ligand for the construction of LanthanideIII coordination polymers and metal-organic frameworks (MOF)[1][2][3].
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1H-pyrazole-3,5-dicarboxylic acid hydrate | 98.0% | 1H-pyrazole-3,5-dicarboxylic acid hydrate (Pyrazole-3,5-dicarboxylic acid monohydrate) serves as a precursor for the synthesis of 26-membered diazatetraester crown ethers and 39-membered triazahexaester crown ethers containing pyrazole units. 1H-pyrazole-3,5-dicarboxylic acid hydrate acts as a V-type heterocyclic polycarboxylic acid bridging ligand for the construction of LanthanideIII coordination polymers and metal-organic frameworks (MOF). | ||||||||||||||||||||
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- [1]. Reviriego F, et al. Hydrogen-bond-mediated self-assembly of 26-membered diaza tetraester crowns of 3,5-disubstituted 1H-pyrazole. Dimerization study in the solid state and in CDCl3 solution. The Journal of organic chemistry. 2011 Oct 21;76(20):8223-31. [Content Brief]
- [2]. Vlasyuk D, et al. Effect of different synthesis approaches on structural and thermal properties of lanthanide (III) metal–organic frameworks based on the 1H-pyrazole-3, 5-dicarboxylate linker[J]. Journal of Inorganic and Organometallic Polymers and Materials, 2021, 31(8): 3534-3548.
- [3]. Alkhnaifes E, et al. Synthesis and Crystal Structure of Two Fe (III) Pyrazole-3, 5-Dicarboxylates[J]. Crystal Growth & Design, 2025, 25(20): 8420-8430.
