4-Cyclopentylidene-3-phenylisoxazol-5(4H)-one CAS 36771-30-9

Purity 97%+In StockPharmaceutical Standards
CAS No.36771-30-9
Molecular FormulaC14H13NO2
Molecular Weight227.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Cyclopentylidene-3-phenylisoxazol-5(4H)-one CAS 36771-30-9 chemical structure

Description

The occurrence of 4-Cyclopentylidene-3-phenylisoxazol-5(4H)-one 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.

4-Cyclopentylidene-3-phenylisoxazol-5(4H)-one (CAS 36771-30-9) is a high-purity analytical reference standard with the molecular formula C14H13NO2 and a molecular weight of 227.26 g/mol.

Based on its molecular formula C14H13NO2, 4-Cyclopentylidene-3-phenylisoxazol-5(4H)-one contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 227.26 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-Cyclopentylidene-3-phenylisoxazol-5(4H)-one 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 FormulaC14H13NO2
Molecular Weight227.26 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1967
Nitrogen Atoms1

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