Methyl 3-(4-bromophenyl)oxirane-2-carboxylate CAS 51622-82-3

Purity 97%+In StockPharmaceutical Standards
CAS No.51622-82-3
Molecular FormulaC10H9BrO3
Molecular Weight257.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(4-bromophenyl)oxirane-2-carboxylate CAS 51622-82-3 chemical structure

Description

CATO manufactures Methyl 3-(4-bromophenyl)oxirane-2-carboxylate 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 Methyl 3-(4-bromophenyl)oxirane-2-carboxylate (CAS 51622-82-3), a certified reference material (molecular formula C10H9BrO3, MW 257.08 g/mol) for analytical method development and quality control.

Based on its molecular formula C10H9BrO3, Methyl 3-(4-bromophenyl)oxirane-2-carboxylate contains a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 257.08 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

Physical & Chemical Properties

Molecular FormulaC10H9BrO3
Molecular Weight257.08 g/mol
AppearanceOff-white to pale 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 methanol, ethanol, 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971
Halogen ContentBr-containing

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