5-(3-Chloro-4-methoxyphenyl)-4-methylisoxazole CAS 1399655-05-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1399655-05-0
Molecular FormulaC11H10ClNO2
Molecular Weight223.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(3-Chloro-4-methoxyphenyl)-4-methylisoxazole CAS 1399655-05-0 chemical structure

Description

CATO supplies 5-(3-Chloro-4-methoxyphenyl)-4-methylisoxazole (CAS 1399655-05-0), a certified reference material (molecular formula C11H10ClNO2, MW 223.66 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H10ClNO2, 5-(3-Chloro-4-methoxyphenyl)-4-methylisoxazole contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 223.66 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 5-(3-Chloro-4-methoxyphenyl)-4-methylisoxazole 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 FormulaC11H10ClNO2
Molecular Weight223.66 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms1

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