3-Cyclopropoxy-2-fluoro-5-iodopyridine CAS 1243421-36-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1243421-36-4
Molecular FormulaC8H7FINO
Molecular Weight279.05 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Cyclopropoxy-2-fluoro-5-iodopyridine CAS 1243421-36-4 chemical structure

Description

CATO supplies 3-Cyclopropoxy-2-fluoro-5-iodopyridine (CAS 1243421-36-4), a certified reference material (molecular formula C8H7FINO, MW 279.05 g/mol) for analytical method development and quality control.

3-Cyclopropoxy-2-fluoro-5-iodopyridine (C8H7FINO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/iodine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

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 3-Cyclopropoxy-2-fluoro-5-iodopyridine 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 FormulaC8H7FINO
Molecular Weight279.05 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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/I-containing
Nitrogen Atoms1

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