3-[5-(Phenoxymethyl)-1,2,4-oxadiazol-3-yl]-benzaldehyde CAS 1119450-79-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1119450-79-1
Molecular FormulaC16H12N2O3
Molecular Weight280.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[5-(Phenoxymethyl)-1,2,4-oxadiazol-3-yl]-benzaldehyde CAS 1119450-79-1 chemical structure

Description

CATO manufactures 3-[5-(Phenoxymethyl)-1,2,4-oxadiazol-3-yl]-benzaldehyde 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-[5-(Phenoxymethyl)-1,2,4-oxadiazol-3-yl]-benzaldehyde (CAS 1119450-79-1), molecular formula C16H12N2O3 and molecular weight 280.28 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 3-[5-(Phenoxymethyl)-1,2,4-oxadiazol-3-yl]-benzaldehyde is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 280.28 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).

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

Physical & Chemical Properties

Molecular FormulaC16H12N2O3
Molecular Weight280.28 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms2

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