1-(4-Fluoro-3-(trifluoromethyl)phenyl)-2,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indol-4-one CAS 1023441-47-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1023441-47-5
Molecular FormulaC18H17F4NO
Molecular Weight339.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Fluoro-3-(trifluoromethyl)phenyl)-2,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indol-4-one CAS 1023441-47-5 chemical structure

Description

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

1-(4-Fluoro-3-(trifluoromethyl)phenyl)-2,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indol-4-one (CAS 1023441-47-5) is a high-purity analytical reference standard with the molecular formula C18H17F4NO and a molecular weight of 339.33 g/mol.

The molecular framework of 1-(4-Fluoro-3-(trifluoromethyl)phenyl)-2,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indol-4-one (C18H17F4NO) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 manufactures 1-(4-Fluoro-3-(trifluoromethyl)phenyl)-2,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indol-4-one 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 FormulaC18H17F4NO
Molecular Weight339.33 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms1

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