4-Chloro-1-(4-fluorophenyl)-N-methyl-1H-pyrazole-5-carboxamide CAS 318949-30-3

Purity 97%+In StockPharmaceutical Standards
CAS No.318949-30-3
Molecular FormulaC11H9ClFN3O
Molecular Weight253.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-1-(4-fluorophenyl)-N-methyl-1H-pyrazole-5-carboxamide CAS 318949-30-3 chemical structure

Description

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

CATO supplies 4-Chloro-1-(4-fluorophenyl)-N-methyl-1H-pyrazole-5-carboxamide (CAS 318949-30-3), a certified reference material (molecular formula C11H9ClFN3O, MW 253.66 g/mol) for analytical method development and quality control.

The molecular framework of 4-Chloro-1-(4-fluorophenyl)-N-methyl-1H-pyrazole-5-carboxamide (C11H9ClFN3O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), 4-Chloro-1-(4-fluorophenyl)-N-methyl-1H-pyrazole-5-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H9ClFN3O
Molecular Weight253.66 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/Cl-containing
Nitrogen Atoms3

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