4-((2-Amino-3-fluorophenyl)amino)cyclohexan-1-ol CAS 1233952-83-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1233952-83-4
Molecular FormulaC12H17FN2O
Molecular Weight224.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-((2-Amino-3-fluorophenyl)amino)cyclohexan-1-ol CAS 1233952-83-4 chemical structure

Description

4-((2-Amino-3-fluorophenyl)amino)cyclohexan-1-ol (C12H17FN2O) 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

4-((2-Amino-3-fluorophenyl)amino)cyclohexan-1-ol (CAS 1233952-83-4) is a high-purity analytical reference standard with the molecular formula C12H17FN2O and a molecular weight of 224.27 g/mol.

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 4-((2-Amino-3-fluorophenyl)amino)cyclohexan-1-ol 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 FormulaC12H17FN2O
Molecular Weight224.27 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms2

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