TERT-BUTYL 5-(TRIFLUOROMETHYL)-1H-INDOLE-1-CARBOXYLATE CAS 351500-12-4

Purity 97%+In StockPharmaceutical Standards
CAS No.351500-12-4
Molecular FormulaC14H14F3NO2
Molecular Weight285.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

TERT-BUTYL 5-(TRIFLUOROMETHYL)-1H-INDOLE-1-CARBOXYLATE CAS 351500-12-4 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.

CATO supplies TERT-BUTYL 5-(TRIFLUOROMETHYL)-1H-INDOLE-1-CARBOXYLATE (CAS 351500-12-4), a certified reference material (molecular formula C14H14F3NO2, MW 285.26 g/mol) for analytical method development and quality control.

The molecular framework of TERT-BUTYL 5-(TRIFLUOROMETHYL)-1H-INDOLE-1-CARBOXYLATE (C14H14F3NO2) is characterized by a nitrogen-containing heterocyclic scaffold, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures TERT-BUTYL 5-(TRIFLUOROMETHYL)-1H-INDOLE-1-CARBOXYLATE 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 FormulaC14H14F3NO2
Molecular Weight285.26 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1

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