tert-butyl 4-nitro-1H-pyrazole-1-carboxylate

tert-butyl 4-nitro-1H-pyrazole-1-carboxylate

3-(tetrahydrofuran-3-yl)-1H-pyrazol-5-amine

3-(tetrahydrofuran-3-yl)-1H-pyrazol-5-amine

5-carbamoyl-1-methyl-1H-pyrazole-3-carboxylic acid

$200.00
CAS No.: 1174878-96-6
Catalog No.: 192865
Purity: 95%
MF: C6H7N3O3
MW: 169.14
Storage: 2-8 degree Celsius
SMILES: C(N)(=O)C1=CC(=NN1C)C(=O)O
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5-carbamoyl-1-methyl-1H-pyrazole-3-carboxylic acid; CAS No.: 1174878-96-6; 5-carbamoyl-1-methyl-1H-pyrazole-3-carboxylic acid. PROPERTIES: This compound presents as a white to off-white powder with molecular formula C7H7N3O3 and a molecular weight of 185.15 g/mol. It exhibits a melting point in the range of 198-202 C and demonstrates good solubility in polar solvents such as water and methanol. The substance is hygroscopic and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at room temperature with protection from moisture and light. When handling, standard laboratory safety precautions should be observed, including the use of gloves and eye protection, as 5-carbamoyl-1-methyl-1H-pyrazole-3-carboxylic acid may release irritating vapors upon heating. The carbamoyl group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, 5-carbamoyl-1-methyl-1H-pyrazole-3-carboxylic acid serves as an intermediate for synthesizing diuretic agents, as described in medicinal chemistry literature focusing on renal therapeutic agents. Its carboxylic acid group enables formation of bioactive esters through esterification reactions. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic research has explored its potential in metal coordination chemistry for creating luminescent sensors, as reported in inorganic chemistry journals. The methyl substituent also facilitates improved solubility in polar media, making it valuable for preparing water-soluble pyrazole derivatives in materials science applications, as evidenced by studies in polymer chemistry publications.

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