1H-indole, 3-iodo-4-(phenylmethoxy)-1-(phenylsulfonyl)- CAS 880872-14-0

Purity 97%+In StockPharmaceutical Standards
CAS No.880872-14-0
Molecular FormulaC21H16INO3S
Molecular Weight489.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1H-indole, 3-iodo-4-(phenylmethoxy)-1-(phenylsulfonyl)- CAS 880872-14-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 489.33 g/mol gives 1H-indole, 3-iodo-4-(phenylmethoxy)-1-(phenylsulfonyl)- distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 1H-indole, 3-iodo-4-(phenylmethoxy)-1-(phenylsulfonyl)- (CAS 880872-14-0), a certified reference material (molecular formula C21H16INO3S, MW 489.33 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution, 1H-indole, 3-iodo-4-(phenylmethoxy)-1-(phenylsulfonyl)- is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 489.33 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

As a certified reference material (CRM), 1H-indole, 3-iodo-4-(phenylmethoxy)-1-(phenylsulfonyl)- meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC21H16INO3S
Molecular Weight489.33 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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