5-(4-Fluorobenzoyl)-3-methylthieno[2,3-c][1,2]thiazol-4-amine CAS 339017-36-6

Purity 97%+In StockPharmaceutical Standards
CAS No.339017-36-6
Molecular FormulaC13H9FN2OS2
Molecular Weight292.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(4-Fluorobenzoyl)-3-methylthieno[2,3-c][1,2]thiazol-4-amine CAS 339017-36-6 chemical structure

Description

Based on its molecular formula C13H9FN2OS2, 5-(4-Fluorobenzoyl)-3-methylthieno[2,3-c][1,2]thiazol-4-amine contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 292.35 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

5-(4-Fluorobenzoyl)-3-methylthieno[2,3-c][1,2]thiazol-4-amine (CAS 339017-36-6) is a high-purity analytical reference standard with the molecular formula C13H9FN2OS2 and a molecular weight of 292.35 g/mol.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures 5-(4-Fluorobenzoyl)-3-methylthieno[2,3-c][1,2]thiazol-4-amine 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 FormulaC13H9FN2OS2
Molecular Weight292.35 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
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 Atoms2
Sulfur Atoms2

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