CAS 663941-72-8
:1H-Pyrazole, 4-bromo-1-(2-chloroethyl)-
Description:
1H-Pyrazole, 4-bromo-1-(2-chloroethyl)- is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of a bromine atom at the 4-position and a chloroethyl group at the 1-position contributes to its reactivity and potential applications in various chemical reactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential use in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of halogen substituents that can influence biological activity. Additionally, the compound may participate in nucleophilic substitution reactions, making it a candidate for further functionalization. Safety data should be consulted, as halogenated compounds can pose health risks, and appropriate handling procedures should be followed. Overall, 1H-Pyrazole, 4-bromo-1-(2-chloroethyl)- is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C5H6BrClN2
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Found 2 products.
4-Bromo-1-(2-chloroethyl)-1H-pyrazole
CAS:Controlled ProductFormula:C5H6BrClN2Color and Shape:NeatMolecular weight:209.4714-Bromo-1-(2-chloroethyl)-1H-pyrazole
CAS:4-Bromo-1-(2-chloroethyl)-1H-pyrazole is a chemical substance that belongs to the group of insensitive explosives. It has been shown to be thermally and geometrically insensitive, with an x-ray structure that is square planar. The techniques used to characterize this compound include XPS, EDS, SEM, and TEM. This compound also has magnetic properties and can be used as a catalyst in Suzuki reactions. 4-Bromo-1-(2-chloroethyl)-1H-pyrazole has been shown to be an efficient photoelectron emission source for microscopy techniques such as diffraction and transfer.Formula:C5H6BrClN2Purity:Min. 95%Molecular weight:209.47 g/mol
