4-(Iodo-phenyl)-methane sulfonyl chloride CAS 345915-64-2

Purity 97%+In StockPharmaceutical Standards
CAS No.345915-64-2
Molecular FormulaC7H6ClIO2S
Molecular Weight316.54 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Iodo-phenyl)-methane sulfonyl chloride CAS 345915-64-2 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 4-(Iodo-phenyl)-methane sulfonyl chloride.

CATO supplies 4-(Iodo-phenyl)-methane sulfonyl chloride (CAS 345915-64-2), a certified reference material (molecular formula C7H6ClIO2S, MW 316.54 g/mol) for analytical method development and quality control.

Based on its molecular formula C7H6ClIO2S, 4-(Iodo-phenyl)-methane sulfonyl chloride contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/iodine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 316.54 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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), 4-(Iodo-phenyl)-methane sulfonyl chloride 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 FormulaC7H6ClIO2S
Molecular Weight316.54 g/mol
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl/I-containing
Sulfur Atoms1

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