2-(3,4-Difluorophenyl)-1H-indole CAS 68290-36-8

Purity 97%+In StockPharmaceutical Standards
CAS No.68290-36-8
Molecular FormulaC14H9F2N
Molecular Weight229.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3,4-Difluorophenyl)-1H-indole CAS 68290-36-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 229.22 g/mol gives 2-(3,4-Difluorophenyl)-1H-indole distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-(3,4-Difluorophenyl)-1H-indole (CAS 68290-36-8), a certified reference material (molecular formula C14H9F2N, MW 229.22 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution, 2-(3,4-Difluorophenyl)-1H-indole is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 229.22 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 2-(3,4-Difluorophenyl)-1H-indole 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 FormulaC14H9F2N
Molecular Weight229.22 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Halogen ContentF-containing
Nitrogen Atoms1

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