4-Cyclopropoxy-2-fluoro-3-(methylthio)pyridine CAS 1243350-43-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1243350-43-7
Molecular FormulaC9H10FNOS
Molecular Weight199.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Cyclopropoxy-2-fluoro-3-(methylthio)pyridine CAS 1243350-43-7 chemical structure

Description

The molecular framework of 4-Cyclopropoxy-2-fluoro-3-(methylthio)pyridine (C9H10FNOS) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, 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.

CATO supplies 4-Cyclopropoxy-2-fluoro-3-(methylthio)pyridine (CAS 1243350-43-7), a certified reference material (molecular formula C9H10FNOS, MW 199.25 g/mol) for analytical method development and quality control.

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

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 FormulaC9H10FNOS
Molecular Weight199.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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