Methyl 2-((3-bromopyridin-4-yl)thio)-2-methylpropanoate CAS 1885097-58-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1885097-58-4
Molecular FormulaC10H12BrNO2S
Molecular Weight290.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-((3-bromopyridin-4-yl)thio)-2-methylpropanoate CAS 1885097-58-4 chemical structure

Description

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.

CATO supplies Methyl 2-((3-bromopyridin-4-yl)thio)-2-methylpropanoate (CAS 1885097-58-4), a certified reference material (molecular formula C10H12BrNO2S, MW 290.18 g/mol) for analytical method development and quality control.

Structurally, Methyl 2-((3-bromopyridin-4-yl)thio)-2-methylpropanoate (C10H12BrNO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 290.18 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

As a certified reference material (CRM), Methyl 2-((3-bromopyridin-4-yl)thio)-2-methylpropanoate 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 FormulaC10H12BrNO2S
Molecular Weight290.18 g/mol
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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