CAS 6994-25-8
:Ethyl 3-amino-1H-pyrazole-4-carboxylate
Description:
Ethyl 3-amino-1H-pyrazole-4-carboxylate is an organic compound characterized by its pyrazole ring structure, which is a five-membered heterocyclic compound containing two nitrogen atoms. This substance features an amino group and an ethyl ester functional group, contributing to its reactivity and potential applications in medicinal chemistry. The presence of the carboxylate group enhances its solubility in polar solvents, making it suitable for various chemical reactions. Ethyl 3-amino-1H-pyrazole-4-carboxylate is often utilized in the synthesis of bioactive molecules and can serve as a building block in the development of pharmaceuticals. Its CAS number, 6994-25-8, allows for easy identification in chemical databases. The compound is typically handled with standard safety precautions, as with many organic chemicals, due to potential toxicity and reactivity. Overall, its unique structural features and functional groups make it a valuable compound in organic synthesis and drug discovery.
Formula:C6H9N3O2
InChI:InChI=1S/C6H9N3O2/c1-2-11-6(10)4-3-8-9-5(4)7/h3H,2H2,1H3,(H3,7,8,9)
InChI key:InChIKey=YPXGHKWOJXQLQU-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(N)=NNC1
Synonyms:- 1H-Pyrazole-4-carboxylic acid, 3-amino-, ethyl ester
- 1H-Pyrazole-4-carboxylic acid, 5-amino-, ethyl ester
- 3-Amino-4-(ethoxycarbonyl)pyrazole
- 3-Amino-4-carbethoxypyrazole
- 3-Amino-4-carboethoxy-2H-pyrazole
- 3-Amino-4-pyrazolecarboxylic acid ethyl ester
- 5-Amino-1H-pyrazole-4-carboxylic acid ethyl ester
- Ethyl 3-amino-1H-pyrazole-4-carboxylate
- Ethyl 3-amino-4-pyarazolecarboxylate
- Ethyl 3-amino-4-pyrazolecarboxylate
- Ethyl 3-aminopyrazol-4-carboxylate
- Ethyl 3-aminopyrazole-4-carboxylate
- Ethyl 5-Amino-1H-4-Pyrazolecarboxylate
- Ethyl 5-amino-1H-pyrazole-4-carboxylate
- Ethyl 5-amino-4-pyrazolecarboxylate
- Ethyl 5-aminopyrazol-4-carboxylate
- Ethyl-5-amino-1H-pyrazol-4-carboxylat
- NSC 521580
- Pyrazole-4-carboxylic acid, 3(or 5)-amino-, ethyl ester
- See more synonyms
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Ethyl 3-Aminopyrazole-4-carboxylate
CAS:Formula:C6H9N3O2Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:155.16Ethyl 3-amino-1H-pyrazole-4-carboxylate, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo SciFormula:C6H9N3O2Purity:99%Color and Shape:White to cream to pale yellow, Crystals or powder or crystalline powderMolecular weight:155.16Allopurinol Related Compound D
CAS:Compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure nesoiFormula:C6H9N3O2Color and Shape:White Light Yellow Crystalline PowderMolecular weight:155.06948Ethyl 3-amino-1H-pyrazole-4-carboxylate
CAS:Ethyl 3-amino-1H-pyrazole-4-carboxylateFormula:C6H9N3O2Purity:≥95%Color and Shape:Off-white Solid-PowderMolecular weight:155.15456Ethyl 5-amino-1H-pyrazole-4-carboxylate
CAS:Ethyl 5-amino-1H-pyrazole-4-carboxylateFormula:C6H9N3O2Purity:>98%Color and Shape:Solid-PowderMolecular weight:155.15456Allopurinol EP Impurity D (Allopurinol USP Related Compound D)
CAS:Formula:C6H9N3O2Color and Shape:Pale Brown SolidMolecular weight:155.16Ethyl 3-Amino-4-pyrazolecarboxylate
CAS:Formula:C6H9N3O2Purity:98%Color and Shape:SolidMolecular weight:155.1546Ethyl 5-Amino-1H-pyrazole-4-carboxylate
CAS:Formula:C6H9N3O2Color and Shape:NeatMolecular weight:155.15Ethyl 3-Amino-4-pyrazolecarboxylate
CAS:Controlled ProductFormula:C6H9N3O2Color and Shape:NeatMolecular weight:155.15Ethyl 3-amino-1H-pyrazole-4-carboxylate
CAS:Ethyl 3-amino-1H-pyrazole-4-carboxylateFormula:C6H9N3O2Purity:95%Molecular weight:155.15Ethyl 3-aminopyrazole-4-carboxylate
CAS:Ethyl 3-aminopyrazole-4-carboxylate is an anticancer drug that inhibits the growth of cancer cells by inhibiting protein synthesis. It has been shown to inhibit the activity of dpp-iv and pde5, which are enzymes involved in cellular proliferation. Ethyl 3-aminopyrazole-4-carboxylate has also been shown to have antiinflammatory properties, which may be due to inhibition of prostaglandin synthesis.
Ethyl 3-aminopyrazole-4-carboxylate is a multinuclear compound that reacts with nitrogen atoms from the pyrazoles to form a stable molecule. Dimethylformamide is used as a solvent for this reaction. The synthesis of ethyl 3-aminopyrazole-4-carboxylate starts with acetylation, which converts the carboxylic acid group into an acetic acid group. The acetic acid group reacts with ammonia and hydrogen cyanFormula:C6H9N3O2Purity:Min. 95%Color and Shape:PowderMolecular weight:155.16 g/mol5-Amino-1H-pyrazole-4-carboxylic acid ethyl ester
CAS:Formula:C6H9N3O2Purity:95%Color and Shape:SolidMolecular weight:155.157
