CAS 50427-77-5

5-amino-1-phenyl-4-pyrazolecarboxamide

Description:

5-amino-1-phenyl-4-pyrazolecarboxamide, with the CAS number 50427-77-5, is a chemical compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group and a phenyl group, contributing to its potential biological activity. It is typically a white to off-white solid and is soluble in polar solvents, which may include water and alcohols, depending on the specific conditions. The presence of the carboxamide functional group enhances its hydrogen bonding capabilities, influencing its reactivity and interaction with biological targets. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry and drug development. Its structural features suggest potential applications in areas such as anti-inflammatory or analgesic therapies, although specific biological activities would require further investigation through experimental studies. As with many organic compounds, proper handling and safety measures should be observed due to potential toxicity or reactivity.

Formula: C₁₀H₁₀N₄O

InChI: InChI=1/C10H10N4O/c11-9-8(10(12)15)6-13-14(9)7-4-2-1-3-5-7/h1-6H,11H2,(H2,12,15)

SMILES: c1ccc(cc1)n1c(c(cn1)C(=N)O)N

Synonyms:

• 5-amino-1-phenyl-1H-pyrazole-4-carboxamide

5-Amino-1-phenyl-1H-pyrazole-4-carboxamide

CAS: 50427-77-5

Formula: C₁₀H₁₀N₄O

Purity: 95%

Color and Shape: Solid

Molecular weight: 202.2126

Ref: IN-DA003MCS

5-Amino-1-phenyl-1H-pyrazole-4-carboxamide

CAS: 50427-77-5

5-Amino-1-phenyl-1H-pyrazole-4-carboxamide

Formula: C₁₀H₁₀N₄O

Purity: ≥95%

Color and Shape: Powder

Molecular weight: 202.21g/mol

Ref: 54-OR12451

5-Amino-1-phenylpyrazole-4-carboxamide

CAS: 50427-77-5

5-Amino-1-phenylpyrazole-4-carboxamide (APC) is a synthetic compound that has been shown to have potential as an antitumor agent. This compound has been shown to inhibit the growth of cancer cells in vitro, with cytometric analysis showing that it inhibits DNA synthesis and cell proliferation. It also has antibacterial activity, which may be due to its ability to inhibit bacterial DNA gyrase and topoisomerase IV. APC has been found in wastewater at concentrations of 2.6 μg/L, indicating that it is currently being produced and used for industrial purposes. APC can be synthesized by reacting 1-(3-aminopropyl)piperazine with 3-(2H)-furanone and triethylamine to form 5-amino-1-[(2H)-pyridin-2-yl]pyrazole-4-- carboxylic acid chloride, which can then

Formula: C₁₀H₁₀N₄O

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 202.21 g/mol

Ref: 3D-FA17420

5-AMINO-1-PHENYL-1H-PYRAZOLE-4-CARBOXAMIDE

CAS: 50427-77-5

Formula: C₁₀H₁₀N₄O

Purity: 95%

Color and Shape: Solid

Molecular weight: 202.217

Ref: 10-F473002

5-Amino-1-phenylpyrazole-4-carboxamide

Controlled Product

CAS: 50427-77-5

Applications Used as a heterocyclic scaffold
References Matysiak, J., et al.: Bioorg. Med. Chem., 11, 2285 (2003), Das, J., et al.: Bioorg. Med. Chem. Lett., 18, 2652 (2008),

Formula: C₁₀H₁₀N₄O

Color and Shape: Neat

Molecular weight: 202.21

Ref: TR-A626225