5-(3-fluorophenyl)-2,3-dihydro-1H-indole hydrochloride CAS 1354959-99-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1354959-99-1
Molecular FormulaC14H12FN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(3-fluorophenyl)-2,3-dihydro-1H-indole hydrochloride CAS 1354959-99-1 chemical structure

Description

CATO supplies 5-(3-fluorophenyl)-2,3-dihydro-1H-indole hydrochloride (CAS 1354959-99-1), a certified reference material (molecular formula C14H12FNHCl, MW 249.71 g/mol) for analytical method development and quality control.

5-(3-fluorophenyl)-2,3-dihydro-1H-indole hydrochloride (C14H12FNHCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/chlorine 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 5-(3-fluorophenyl)-2,3-dihydro-1H-indole hydrochloride 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 FormulaC14H12FN HCl
Molecular Weight249.71 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
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.)1991
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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