5-(4-Bromophenyl)-3-methyl-1H-pyrazole


Chemical Name: 5-(4-Bromophenyl)-3-methyl-1H-pyrazole
CAS Number: 948293-34-3
Product Number: AG00IIKK(AGN-PC-0WAIFT)
Synonyms:
MDL No:
Molecular Formula: C10H9BrN2
Molecular Weight: 237.09586

Identification/Properties


Computed Properties
Molecular Weight:
237.1g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
235.995g/mol
Monoisotopic Mass:
235.995g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
166
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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Chemical Structure



5-(4-Bromophenyl)-3-methyl-1H-pyrazole, also known as $name$, is a versatile compound widely used in chemical synthesis. With its unique structure and reactivity, this compound serves as a key building block in the synthesis of various organic molecules. In particular, $name$ is commonly employed as a precursor in the preparation of pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, $name$ plays a crucial role as a heterocyclic scaffold, allowing for the introduction of functional groups and modifications to yield desired products. Its bromophenyl and methyl substituents provide opportunities for further derivatization, enabling the creation of structurally diverse compounds with tailored properties. Chemists utilize $name$ as a starting material or intermediate in the synthesis of biologically active compounds, polymers, and other complex molecules.Moreover, the presence of the pyrazole ring in $name$ offers unique reactivity and potential for diverse transformations in organic synthesis. This allows for the creation of novel compounds with specific characteristics or activities, making $name$ a valuable tool in the hands of synthetic chemists. Overall, the application of 5-(4-Bromophenyl)-3-methyl-1H-pyrazole in chemical synthesis demonstrates its significance as a versatile building block for the efficient and strategic construction of organic molecules.