4-(3-(Trifluoromethyl)benzyl)-2H-benzo[b][1,4]thiazin-3(4H)-one CAS 353262-04-1

Purity 97%+In StockPharmaceutical Standards
CAS No.353262-04-1
Molecular FormulaC16H12F3NOS
Molecular Weight323.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-(Trifluoromethyl)benzyl)-2H-benzo[b][1,4]thiazin-3(4H)-one CAS 353262-04-1 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-(3-(Trifluoromethyl)benzyl)-2H-benzo[b][1,4]thiazin-3(4H)-one (CAS 353262-04-1), molecular formula C16H12F3NOS and molecular weight 323.33 g/mol, is a CATO reference standard with documented purity and traceability.

4-(3-(Trifluoromethyl)benzyl)-2H-benzo[b][1,4]thiazin-3(4H)-one (C16H12F3NOS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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-(3-(Trifluoromethyl)benzyl)-2H-benzo[b][1,4]thiazin-3(4H)-one 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 FormulaC16H12F3NOS
Molecular Weight323.33 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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