3-(4-(2,2,3,3-Tetrafluoropropoxy)phenyl)acrylonitrile CAS 123632-23-5

Purity 97%+In StockPharmaceutical Standards
CAS No.123632-23-5
Molecular FormulaC12H9F4NO
Molecular Weight259.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-(2,2,3,3-Tetrafluoropropoxy)phenyl)acrylonitrile CAS 123632-23-5 chemical structure

Description

3-(4-(2,2,3,3-Tetrafluoropropoxy)phenyl)acrylonitrile (C12H9F4NO) 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 3-(4-(2,2,3,3-Tetrafluoropropoxy)phenyl)acrylonitrile (CAS 123632-23-5), a certified reference material (molecular formula C12H9F4NO, MW 259.20 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.

CATO manufactures 3-(4-(2,2,3,3-Tetrafluoropropoxy)phenyl)acrylonitrile 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 FormulaC12H9F4NO
Molecular Weight259.20 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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.)1992
Halogen ContentF-containing
Nitrogen Atoms1

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