N-[4-cyano-2-iodo-5-(trifluoromethyl)phenyl]methanesulfonamide CAS 868692-62-0

Purity 97%+In StockPharmaceutical Standards
CAS No.868692-62-0
Molecular FormulaC9H6F3IN2O2S
Molecular Weight390.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-[4-cyano-2-iodo-5-(trifluoromethyl)phenyl]methanesulfonamide CAS 868692-62-0 chemical structure

Description

Based on its molecular formula C9H6F3IN2O2S, N-[4-cyano-2-iodo-5-(trifluoromethyl)phenyl]methanesulfonamide contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 390.12 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

N-[4-cyano-2-iodo-5-(trifluoromethyl)phenyl]methanesulfonamide (CAS 868692-62-0) is a high-purity analytical reference standard with the molecular formula C9H6F3IN2O2S and a molecular weight of 390.12 g/mol.

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), N-[4-cyano-2-iodo-5-(trifluoromethyl)phenyl]methanesulfonamide 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 FormulaC9H6F3IN2O2S
Molecular Weight390.12 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/I-containing
Nitrogen Atoms2
Sulfur Atoms1

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