3-((3-(Trifluoromethyl)benzyl)thio)-4H-benzo[b][1,4]thiazine 1,1-dioxide CAS 477868-88-5

Purity 97%+In StockPharmaceutical Standards
CAS No.477868-88-5
Molecular FormulaC16H12F3NO2S2
Molecular Weight371.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((3-(Trifluoromethyl)benzyl)thio)-4H-benzo[b][1,4]thiazine 1,1-dioxide CAS 477868-88-5 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.

3-((3-(Trifluoromethyl)benzyl)thio)-4H-benzo[b][1,4]thiazine 1,1-dioxide (CAS 477868-88-5) is a high-purity analytical reference standard with the molecular formula C16H12F3NO2S2 and a molecular weight of 371.40 g/mol.

3-((3-(Trifluoromethyl)benzyl)thio)-4H-benzo[b][1,4]thiazine 1,1-dioxide (C16H12F3NO2S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, 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, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 3-((3-(Trifluoromethyl)benzyl)thio)-4H-benzo[b][1,4]thiazine 1,1-dioxide 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 FormulaC16H12F3NO2S2
Molecular Weight371.40 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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