Methyl 5,6-difluoro-3-iodo-1H-indole-2-carboxylate CAS 1415394-13-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1415394-13-6
Molecular FormulaC10H6F2INO2
Molecular Weight337.06 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 5,6-difluoro-3-iodo-1H-indole-2-carboxylate CAS 1415394-13-6 chemical structure

Description

CATO manufactures Methyl 5,6-difluoro-3-iodo-1H-indole-2-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.

Methyl 5,6-difluoro-3-iodo-1H-indole-2-carboxylate (CAS 1415394-13-6), molecular formula C10H6F2INO2 and molecular weight 337.06 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of Methyl 5,6-difluoro-3-iodo-1H-indole-2-carboxylate (C10H6F2INO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/iodine 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC10H6F2INO2
Molecular Weight337.06 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
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.)1991
Halogen ContentF/I-containing
Nitrogen Atoms1

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