2-((3-Chloro-4-fluorophenyl)amino)-4H-[1,3]thiazino[5,6-b]quinoxalin-4-one CAS 154371-22-9

Purity 97%+In StockPharmaceutical Standards
CAS No.154371-22-9
Molecular FormulaC16H8ClFN4OS
Molecular Weight358.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((3-Chloro-4-fluorophenyl)amino)-4H-[1,3]thiazino[5,6-b]quinoxalin-4-one CAS 154371-22-9 chemical structure

Description

2-((3-Chloro-4-fluorophenyl)amino)-4H-[1,3]thiazino[5,6-b]quinoxalin-4-one (CAS 154371-22-9), molecular formula C16H8ClFN4OS and molecular weight 358.78 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, 2-((3-Chloro-4-fluorophenyl)amino)-4H-[1,3]thiazino[5,6-b]quinoxalin-4-one is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 358.78 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 2-((3-Chloro-4-fluorophenyl)amino)-4H-[1,3]thiazino[5,6-b]quinoxalin-4-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 FormulaC16H8ClFN4OS
Molecular Weight358.78 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2001
Halogen ContentF/Cl-containing
Nitrogen Atoms4
Sulfur Atoms1

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