4-(2,3,4-Trifluorobenzenesulfonamidomethyl)benzoic acid CAS 794559-15-2

Purity 97%+In StockPharmaceutical Standards
CAS No.794559-15-2
Molecular FormulaC14H10F3NO4S
Molecular Weight345.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(2,3,4-Trifluorobenzenesulfonamidomethyl)benzoic acid CAS 794559-15-2 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

4-(2,3,4-Trifluorobenzenesulfonamidomethyl)benzoic acid (CAS 794559-15-2) is a high-purity analytical reference standard with the molecular formula C14H10F3NO4S and a molecular weight of 345.29 g/mol.

Structurally, 4-(2,3,4-Trifluorobenzenesulfonamidomethyl)benzoic acid (C14H10F3NO4S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 345.29 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures 4-(2,3,4-Trifluorobenzenesulfonamidomethyl)benzoic acid 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 FormulaC14H10F3NO4S
Molecular Weight345.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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