2-Ethyl-1,3-oxazole-4-carbonyl chloride CAS 1858241-93-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1858241-93-6
Molecular FormulaC6H6ClNO2
Molecular Weight159.57 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Ethyl-1,3-oxazole-4-carbonyl chloride CAS 1858241-93-6 chemical structure

Description

CATO manufactures 2-Ethyl-1,3-oxazole-4-carbonyl chloride 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.

CATO supplies 2-Ethyl-1,3-oxazole-4-carbonyl chloride (CAS 1858241-93-6), a certified reference material (molecular formula C6H6ClNO2, MW 159.57 g/mol) for analytical method development and quality control.

Based on its molecular formula C6H6ClNO2, 2-Ethyl-1,3-oxazole-4-carbonyl chloride contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 159.57 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 FormulaC6H6ClNO2
Molecular Weight159.57 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms1

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