6994-25-8
6994-25-8
Chemical Structure
Ethyl 3-amino-1H-pyrazole-4-carboxylate
Synonym(s): 3-Amino-4-ethoxycarbonylpyrazole
- CAS No.: 6994-25-8
- Formula:C6H9N3O2
- Molecular Weight:155.16
IUPAC Name: ethyl 3-amino-1H-pyrazole-4-carboxylate
InChIKey: YPXGHKWOJXQLQU-UHFFFAOYSA-N
SMILES: CCOC(C1=CNN=C1N)=O
Biological Activity: Ethyl 3-amino-1H-pyrazole-4-carboxylate (3-Amino-4-ethoxycarbonylpyrazole) is a diamagnetic pyrazole derivative ligand. Ethyl 3-amino-1H-pyrazole-4-carboxylate can form copper bromide coordination compounds. Ethyl 3-amino-1H-pyrazole-4-carboxylate serves as a ligand for the synthesis of metal coordination compounds[1][2].
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Ethyl 3-amino-1H-pyrazole-4-carboxylate | 99.55% | Ethyl 3-amino-1H-pyrazole-4-carboxylate (3-Amino-4-ethoxycarbonylpyrazole) is a diamagnetic pyrazole derivative ligand. Ethyl 3-amino-1H-pyrazole-4-carboxylate can form copper bromide coordination compounds. Ethyl 3-amino-1H-pyrazole-4-carboxylate serves as a ligand for the synthesis of metal coordination compounds. | ||||||||||||||||||||
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Ethyl 3-amino-1H-pyrazole-4-carboxylate (Standard) | ≥98% | Ethyl 3-amino-1H-pyrazole-4-carboxylate (Standard) (3-Amino-4-ethoxycarbonylpyrazole (Standard)) is the analytical standard of Ethyl 3-amino-1H-pyrazole-4-carboxylate (HY-W007997). This product is intended for research and analytical applications. Ethyl 3-amino-1H-pyrazole-4-carboxylate (3-Amino-4-ethoxycarbonylpyrazole) is a diamagnetic pyrazole derivative ligand. Ethyl 3-amino-1H-pyrazole-4-carboxylate can form copper bromide coordination compounds. Ethyl 3-amino-1H-pyrazole-4-carboxylate serves as a ligand for the synthesis of metal coordination compounds. | ||||||||||||||||||||
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References
- [1]. Berezin A S, et al. Synthesis, Structure, and Properties of a Copper Bromide Coordination Compound with 3-Amino-4-EthoxyCarbonylPyrazole. Nature of the Nonresonant and Ferromagnetic Absorption Observed by EPR[J]. Journal of Superconductivity and Novel Magnetism, 2015, 28(3): 1007-1011.
- [2]. Huard K, et al. Synthesis of spiropiperidine lactam acetyl-CoA carboxylase inhibitors. The Journal of organic chemistry. 2012 Nov 16;77(22):10050-7.
