2-(3-Bromo-phenyl)-oxazole-4-carboxylic acid ethyl ester CAS 885273-06-3

Purity 97%+In StockPharmaceutical Standards
CAS No.885273-06-3
Molecular FormulaC12H10BrNO3
Molecular Weight296.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-Bromo-phenyl)-oxazole-4-carboxylic acid ethyl ester CAS 885273-06-3 chemical structure

Description

2-(3-Bromo-phenyl)-oxazole-4-carboxylic acid ethyl ester (CAS 885273-06-3) is a high-purity analytical reference standard with the molecular formula C12H10BrNO3 and a molecular weight of 296.12 g/mol.

Structurally, 2-(3-Bromo-phenyl)-oxazole-4-carboxylic acid ethyl ester (C12H10BrNO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 296.12 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 2-(3-Bromo-phenyl)-oxazole-4-carboxylic acid ethyl ester 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 FormulaC12H10BrNO3
Molecular Weight296.12 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, 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; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentBr-containing
Nitrogen Atoms1

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