4-[(1,5-dimethyl-1H-pyrazol-4-yl)methoxy]-3-fluoroaniline CAS 1006961-04-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1006961-04-1
Molecular FormulaC12H14FN3O
Molecular Weight235.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-[(1,5-dimethyl-1H-pyrazol-4-yl)methoxy]-3-fluoroaniline CAS 1006961-04-1 chemical structure

Description

4-[(1,5-dimethyl-1H-pyrazol-4-yl)methoxy]-3-fluoroaniline (C12H14FN3O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 4-[(1,5-dimethyl-1H-pyrazol-4-yl)methoxy]-3-fluoroaniline (CAS 1006961-04-1), a certified reference material (molecular formula C12H14FN3O, MW 235.26 g/mol) for analytical method development and quality control.

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.

As a certified reference material (CRM), 4-[(1,5-dimethyl-1H-pyrazol-4-yl)methoxy]-3-fluoroaniline 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 FormulaC12H14FN3O
Molecular Weight235.26 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.)1988
Halogen ContentF-containing
Nitrogen Atoms3

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