CAS 141302-33-2
:1H-Pyrazole, 4-bromo-1-propyl-
Description:
1H-Pyrazole, 4-bromo-1-propyl- is an organic compound characterized by its pyrazole ring structure, which consists of a five-membered ring containing two adjacent nitrogen atoms. The presence of a bromine atom at the 4-position of the pyrazole ring introduces a halogen substituent, which can influence the compound's reactivity and physical properties. The propyl group at the 1-position contributes to the hydrophobic character of the molecule, affecting its solubility in various solvents. This compound may exhibit biological activity, making it of interest in medicinal chemistry and agrochemicals. Its molecular structure allows for potential interactions with biological targets, and the bromine substituent can enhance its lipophilicity. The compound's properties, such as melting point, boiling point, and spectral characteristics, would typically be determined through experimental methods. Overall, 1H-Pyrazole, 4-bromo-1-propyl- is a versatile compound with potential applications in various fields, including pharmaceuticals and materials science.
Formula:C6H9BrN2
Synonyms:- 4-bromo-1-propyl-1H-pyrazole
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Found 4 products.
4-Bromo-1-propyl-1H-pyrazole
CAS:Formula:C6H9BrN2Purity:97%Color and Shape:LiquidMolecular weight:189.05314-Bromo-1-propyl-1H-pyrazole
CAS:<p>4-Bromo-1-propyl-1H-pyrazole</p>Purity:98%Molecular weight:189.05g/mol4-Bromo-1-propyl-1H-pyrazole
CAS:Formula:C6H9BrN2Purity:≥97%Color and Shape:LiquidMolecular weight:189.0564-Bromo-1-propyl-1H-pyrazole
CAS:<p>4-Bromo-1-propyl-1H-pyrazole is a pyrazole derivative. It is synthesized from the reaction of 4-bromobenzaldehyde and propyl hydrazine, followed by reduction with sodium borohydride. This compound has been shown to be effective against E. coli in an express test. The mechanism of action for this compound is not yet known.</p>Formula:C6H9BrN2Purity:Min. 95%Molecular weight:189.06 g/mol



