n-(2-Chlorophenyl)-3-(5-mercapto-4-phenyl-4h-1,2,4-triazol-3-yl)benzenesulfonamide CAS 748776-60-5

Purity 97%+In StockPharmaceutical Standards
CAS No.748776-60-5
Molecular FormulaC20H15ClN4O2S2
Molecular Weight442.94 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(2-Chlorophenyl)-3-(5-mercapto-4-phenyl-4h-1,2,4-triazol-3-yl)benzenesulfonamide CAS 748776-60-5 chemical structure

Description

n-(2-Chlorophenyl)-3-(5-mercapto-4-phenyl-4h-1,2,4-triazol-3-yl)benzenesulfonamide (CAS 748776-60-5) is a high-purity analytical reference standard with the molecular formula C20H15ClN4O2S2 and a molecular weight of 442.94 g/mol.

Structurally, n-(2-Chlorophenyl)-3-(5-mercapto-4-phenyl-4h-1,2,4-triazol-3-yl)benzenesulfonamide (C20H15ClN4O2S2) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 15.0, corresponding to approximately 15 ring(s) or double-bond equivalent(s). With a molecular weight of 442.94 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 n-(2-Chlorophenyl)-3-(5-mercapto-4-phenyl-4h-1,2,4-triazol-3-yl)benzenesulfonamide 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 FormulaC20H15ClN4O2S2
Molecular Weight442.94 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms2

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