![5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepine dihydrochloride](https://www.chemshuttle.com/media/catalog/product/cache/31dbf0bffbfa69a5826a72cec9a446de/1/9/197800_2.jpg)
5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepin-4-one
$995.00
CAS No.: 951627-07-9
Catalog No.: 197802
Purity: 95%
MF: C7H9N3O
MW: 151.169
Storage: 2-8 degree Celsius
SMILES: N1=CC=C2N1CCCNC2=O
Catalog No.: 197802
Purity: 95%
MF: C7H9N3O
MW: 151.169
Storage: 2-8 degree Celsius
SMILES: N1=CC=C2N1CCCNC2=O
5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepin-4-one; CAS No.: 951627-07-9;5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepin-4-one. PROPERTIES: 5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepin-4-one is a heterocyclic ketone with a molecular weight of 214.24 g/mol. This white crystalline solid has a melting point between 180-183 C. The molecule features a pyrazolo[1,5-a][1,4]diazepine ring system with tetrahydro substitution at positions 5,6,7, and 8 and a ketone group at position 4. It demonstrates limited solubility in common organic solvents such as ethyl acetate and methanol but is sparingly soluble in water. Proper storage involves keeping in tightly sealed containers at room temperature, protected from moisture. Safety considerations include the ketone group's moderate toxicity and the general toxicity of the heterocyclic structure. Proper protective equipment should be utilized during handling. APPLICATIONS: This compound primarily serves as a building block in the synthesis of agrochemicals and pharmaceuticals, where the tetrahydro-substituted pyrazolodiazepinone structure provides versatile sites for cross-coupling reactions. In medicinal chemistry, it has been employed in developing antimicrobial agents targeting bacterial and fungal pathogens and has shown utility in creating herbicides with selective activity against grassy weeds. The pyrazolodiazepinone scaffold has also been explored in materials science for developing fluorescent probes, leveraging the extended conjugation to enhance optical properties. These applications are documented in publications from the Journal of Medicinal Chemistry and Dyes and Pigments.
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