3-(1,4-Dioxaspiro[4.5]Dec-7-en-8-yl)-1-(3-(trifluoromethyl)benzyl)-1H-indole CAS 882747-56-0

Purity 97%+In StockPharmaceutical Standards
CAS No.882747-56-0
Molecular FormulaC24H22F3NO2
Molecular Weight413.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(1,4-Dioxaspiro[4.5]Dec-7-en-8-yl)-1-(3-(trifluoromethyl)benzyl)-1H-indole CAS 882747-56-0 chemical structure

Description

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, 3-(1,4-Dioxaspiro[4.5]Dec-7-en-8-yl)-1-(3-(trifluoromethyl)benzyl)-1H-indole is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 413.43 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

CATO supplies 3-(1,4-Dioxaspiro[4.5]Dec-7-en-8-yl)-1-(3-(trifluoromethyl)benzyl)-1H-indole (CAS 882747-56-0), a certified reference material (molecular formula C24H22F3NO2, MW 413.43 g/mol) for analytical method development and quality control.

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 3-(1,4-Dioxaspiro[4.5]Dec-7-en-8-yl)-1-(3-(trifluoromethyl)benzyl)-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 FormulaC24H22F3NO2
Molecular Weight413.43 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1

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