4-Fluoropyridine-2-carboxaldehyde CAS 1060809-18-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1060809-18-8
Molecular FormulaC6H4FNO
Molecular Weight125.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Fluoropyridine-2-carboxaldehyde CAS 1060809-18-8 chemical structure

Description

The occurrence of 4-Fluoropyridine-2-carboxaldehyde is closely related to an amide group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

4-Fluoropyridine-2-carboxaldehyde (CAS 1060809-18-8), molecular formula C6H4FNO and molecular weight 125.10 g/mol, is a CATO reference standard with documented purity and traceability.

4-Fluoropyridine-2-carboxaldehyde (C6H4FNO) contains an amide group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. 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 4-Fluoropyridine-2-carboxaldehyde 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 FormulaC6H4FNO
Molecular Weight125.10 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.)1988
Halogen ContentF-containing
Nitrogen Atoms1

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