Methyl 3-[(4-Bromophenyl)(hydroxy)methyl]isoxazole-4-carboxylate CAS 2006277-99-0

Purity 97%+In StockPharmaceutical Standards
CAS No.2006277-99-0
Molecular FormulaC12H10BrNO4
Molecular Weight312.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-[(4-Bromophenyl)(hydroxy)methyl]isoxazole-4-carboxylate CAS 2006277-99-0 chemical structure

Description

Based on its molecular formula C12H10BrNO4, Methyl 3-[(4-Bromophenyl)(hydroxy)methyl]isoxazole-4-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 312.12 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies Methyl 3-[(4-Bromophenyl)(hydroxy)methyl]isoxazole-4-carboxylate (CAS 2006277-99-0), a certified reference material (molecular formula C12H10BrNO4, MW 312.12 g/mol) for analytical method development and quality control.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), Methyl 3-[(4-Bromophenyl)(hydroxy)methyl]isoxazole-4-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC12H10BrNO4
Molecular Weight312.12 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
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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.)1996
Halogen ContentBr-containing
Nitrogen Atoms1

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