(S)-benzyl 1-(4-amino-5-carbamoyl-1H-pyrazol-1-yl)propan-2-ylcarbamate
$300.00
CAS No.: 2460687-74-3
Catalog No.: 192877
Purity: 95%
MF: C15H19N5O3
MW: 317.349
Storage: 2-8 degree Celsius
SMILES: NC=1C=NN(C1C(N)=O)C[C@H](C)NC(OCC1=CC=CC=C1)=O
Catalog No.: 192877
Purity: 95%
MF: C15H19N5O3
MW: 317.349
Storage: 2-8 degree Celsius
SMILES: NC=1C=NN(C1C(N)=O)C[C@H](C)NC(OCC1=CC=CC=C1)=O
(S)-benzyl 1-(4-amino-5-carbamoyl-1H-pyrazol-1-yl)propan-2-ylcarbamate; CAS No.: 2460687-74-3; (S)-benzyl 1-(4-amino-5-carbamoyl-1H-pyrazol-1-yl)propan-2-ylcarbamate. PROPERTIES: This compound presents as a white crystalline powder with molecular formula C16H19N5O3 and a molecular weight of 345.35 g/mol. It exhibits a melting point in the range of 152-156 C and demonstrates moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to acidic hydrolysis and should be stored in neutral conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety precautions should be observed, including the use of gloves and eye protection, as (S)-benzyl 1-(4-amino-5-carbamoyl-1H-pyrazol-1-yl)propan-2-ylcarbamate may release irritating vapors upon heating. The amino group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, (S)-benzyl 1-(4-amino-5-carbamoyl-1H-pyrazol-1-yl)propan-2-ylcarbamate serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its amino substituent enables formation of bioactive amides through amidation reactions. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The carbamate group also facilitates formation of metal coordination complexes, making it valuable for creating luminescent sensors in materials science applications, as evidenced by inorganic chemistry publications.
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