4-(Chloromethyl)-5-methyl-1-phenyl-1H-pyrazole CAS 728913-75-5

Purity 97%+In StockPharmaceutical Standards
CAS No.728913-75-5
Molecular FormulaC11H11ClN2
Molecular Weight206.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Chloromethyl)-5-methyl-1-phenyl-1H-pyrazole CAS 728913-75-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 206.67 g/mol gives 4-(Chloromethyl)-5-methyl-1-phenyl-1H-pyrazole distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-(Chloromethyl)-5-methyl-1-phenyl-1H-pyrazole (CAS 728913-75-5) is a high-purity analytical reference standard with the molecular formula C11H11ClN2 and a molecular weight of 206.67 g/mol.

4-(Chloromethyl)-5-methyl-1-phenyl-1H-pyrazole (C11H11ClN2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 4-(Chloromethyl)-5-methyl-1-phenyl-1H-pyrazole under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC11H11ClN2
Molecular Weight206.67 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms2

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