4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline CAS 10364-76-8

Purity 97%+In StockPharmaceutical Standards
CAS No.10364-76-8
Molecular FormulaC11H13N3O
Molecular Weight203.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline CAS 10364-76-8 chemical structure

Description

The occurrence of 4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline (CAS 10364-76-8), a certified reference material (molecular formula C11H13N3O, MW 203.24 g/mol) for analytical method development and quality control.

Structurally, 4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline (C11H13N3O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 203.24 g/mol, it falls into the medium-molecular-weight range. 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-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline 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 FormulaC11H13N3O
Molecular Weight203.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959
Nitrogen Atoms3

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