3-tert-Butyl-1-(2-chlorophenyl)-1h-pyrazole-4-carbaldehyde CAS 1154284-12-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1154284-12-4
Molecular FormulaC14H15ClN2O
Molecular Weight262.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-tert-Butyl-1-(2-chlorophenyl)-1h-pyrazole-4-carbaldehyde CAS 1154284-12-4 chemical structure

Description

CATO supplies 3-tert-Butyl-1-(2-chlorophenyl)-1h-pyrazole-4-carbaldehyde (CAS 1154284-12-4), a certified reference material (molecular formula C14H15ClN2O, MW 262.73 g/mol) for analytical method development and quality control.

The molecular framework of 3-tert-Butyl-1-(2-chlorophenyl)-1h-pyrazole-4-carbaldehyde (C14H15ClN2O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures 3-tert-Butyl-1-(2-chlorophenyl)-1h-pyrazole-4-carbaldehyde 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 FormulaC14H15ClN2O
Molecular Weight262.73 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.)1989
Halogen ContentCl-containing
Nitrogen Atoms2

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