5-(tert-butyl) 2-ethyl 3-bromo-7,8-dihydro-4H-pyrazolo[1,5-a][1,4]diazepine-2,5(6H)-dicarboxylate

5-(tert-butyl) 2-ethyl 3-bromo-7,8-dihydro-4H-pyrazolo[1,5-a][1,4]diazepine-2,5(6H)-dicarboxylate

2-(p-tolyl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepine

2-(p-tolyl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepine

2-(pyridin-4-yl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepine

$345.00
CAS No.: 1340875-61-7
Catalog No.: 197787
Purity: 95%
MF: C12H14N4
MW: 214.272
Storage: 2-8 degree Celsius
SMILES: N1=CC=C(C=C1)C1=NN2C(CNCCC2)=C1
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2-(pyridin-4-yl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepine; CAS No.: 1340875-61-7;2-(pyridin-4-yl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepine. PROPERTIES: 2-(pyridin-4-yl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,4]diazepine is a pyridine-substituted heterocycle with a molecular weight of 259.29 g/mol. This white crystalline solid has a melting point between 155-158 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 pyridin-4-yl group at position 2. It demonstrates limited solubility in common organic solvents such as methanol and acetone but is sparingly soluble in water. Proper storage involves keeping in tightly sealed containers at room temperature, protected from moisture. Safety considerations include the amine groups' potential to cause skin irritation and the pyridine group's general toxicity. 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 pyridine-substituted pyrazolodiazepine structure provides essential binding affinity to target enzymes. 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 pyrazolodiazepine-pyridine structure 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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