1-(Benzenesulfonyl)-6-iodo-2-methyl-1H-indole CAS 1818847-55-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1818847-55-0
Molecular FormulaC15H12INO2S
Molecular Weight397.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(Benzenesulfonyl)-6-iodo-2-methyl-1H-indole CAS 1818847-55-0 chemical structure

Description

The occurrence of 1-(Benzenesulfonyl)-6-iodo-2-methyl-1H-indole is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1-(Benzenesulfonyl)-6-iodo-2-methyl-1H-indole (CAS 1818847-55-0), a certified reference material (molecular formula C15H12INO2S, MW 397.23 g/mol) for analytical method development and quality control.

The molecular framework of 1-(Benzenesulfonyl)-6-iodo-2-methyl-1H-indole (C15H12INO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 1-(Benzenesulfonyl)-6-iodo-2-methyl-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 FormulaC15H12INO2S
Molecular Weight397.23 g/mol
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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