N-(4-Methoxyphenyl)-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfanyl]benzamide CAS 672951-87-0

Purity 97%+In StockPharmaceutical Standards
CAS No.672951-87-0
Molecular FormulaC18H16F3NO2S
Molecular Weight367.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Methoxyphenyl)-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfanyl]benzamide CAS 672951-87-0 chemical structure

Description

The molecular framework of N-(4-Methoxyphenyl)-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfanyl]benzamide (C18H16F3NO2S) 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

N-(4-Methoxyphenyl)-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfanyl]benzamide (CAS 672951-87-0), molecular formula C18H16F3NO2S and molecular weight 367.39 g/mol, is a CATO reference standard with documented purity and traceability.

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 N-(4-Methoxyphenyl)-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfanyl]benzamide 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 FormulaC18H16F3NO2S
Molecular Weight367.39 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

Related N Standards

Recommended Standards

Why CATO?