(3-Fluoro-4-methoxyphenyl)(7-(thiophen-2-yl)-1,4-thiazepan-4-yl)methanone CAS 1706183-49-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1706183-49-4
Molecular FormulaC17H18FNO2S2
Molecular Weight351.46 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-Fluoro-4-methoxyphenyl)(7-(thiophen-2-yl)-1,4-thiazepan-4-yl)methanone CAS 1706183-49-4 chemical structure

Description

CATO manufactures (3-Fluoro-4-methoxyphenyl)(7-(thiophen-2-yl)-1,4-thiazepan-4-yl)methanone 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.

(3-Fluoro-4-methoxyphenyl)(7-(thiophen-2-yl)-1,4-thiazepan-4-yl)methanone (CAS 1706183-49-4), molecular formula C17H18FNO2S2 and molecular weight 351.46 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, (3-Fluoro-4-methoxyphenyl)(7-(thiophen-2-yl)-1,4-thiazepan-4-yl)methanone is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 351.46 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC17H18FNO2S2
Molecular Weight351.46 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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