(E)-4-(2-(thiophen-2-yl)vinyl)-8-(trifluoromethoxy)-2,3-dihydrothieno[3,2-c]quinoline CAS 866133-43-9

Purity 97%+In StockPharmaceutical Standards
CAS No.866133-43-9
Molecular FormulaC18H12F3NOS2
Molecular Weight379.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-4-(2-(thiophen-2-yl)vinyl)-8-(trifluoromethoxy)-2,3-dihydrothieno[3,2-c]quinoline CAS 866133-43-9 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.

(E)-4-(2-(thiophen-2-yl)vinyl)-8-(trifluoromethoxy)-2,3-dihydrothieno[3,2-c]quinoline (CAS 866133-43-9), molecular formula C18H12F3NOS2 and molecular weight 379.42 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (E)-4-(2-(thiophen-2-yl)vinyl)-8-(trifluoromethoxy)-2,3-dihydrothieno[3,2-c]quinoline (C18H12F3NOS2) is characterized by a steroid core, an amide group, sulfur-containing functionality, 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC18H12F3NOS2
Molecular Weight379.42 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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