8-Methyl-N-(4-(trifluoromethoxy)phenyl)-4H-thieno[3,2-c]thiochromene-2-carboxamide CAS 477887-29-9

Purity 97%+In StockPharmaceutical Standards
CAS No.477887-29-9
Molecular FormulaC20H14F3NO2S2
Molecular Weight421.46 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-Methyl-N-(4-(trifluoromethoxy)phenyl)-4H-thieno[3,2-c]thiochromene-2-carboxamide CAS 477887-29-9 chemical structure

Description

As a certified reference material (CRM), 8-Methyl-N-(4-(trifluoromethoxy)phenyl)-4H-thieno[3,2-c]thiochromene-2-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

8-Methyl-N-(4-(trifluoromethoxy)phenyl)-4H-thieno[3,2-c]thiochromene-2-carboxamide (CAS 477887-29-9) is a high-purity analytical reference standard with the molecular formula C20H14F3NO2S2 and a molecular weight of 421.46 g/mol.

The molecular framework of 8-Methyl-N-(4-(trifluoromethoxy)phenyl)-4H-thieno[3,2-c]thiochromene-2-carboxamide (C20H14F3NO2S2) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

Physical & Chemical Properties

Molecular FormulaC20H14F3NO2S2
Molecular Weight421.46 g/mol
Purity97%+
StorageStore at room temperature, 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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

Recommended Standards

Why CATO?