6-(Trifluoromethyl)-1H-indole-5-carboxylic acid CAS 2091850-39-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2091850-39-2
Molecular FormulaC10H6F3NO2
Molecular Weight229.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(Trifluoromethyl)-1H-indole-5-carboxylic acid CAS 2091850-39-2 chemical structure

Description

CATO manufactures 6-(Trifluoromethyl)-1H-indole-5-carboxylic acid 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.

6-(Trifluoromethyl)-1H-indole-5-carboxylic acid (CAS 2091850-39-2), molecular formula C10H6F3NO2 and molecular weight 229.16 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 6-(Trifluoromethyl)-1H-indole-5-carboxylic acid (C10H6F3NO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 229.16 g/mol, it falls into the medium-molecular-weight range. 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.

Physical & Chemical Properties

Molecular FormulaC10H6F3NO2
Molecular Weight229.16 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-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.)1997
Halogen ContentF-containing
Nitrogen Atoms1

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