5-(2-Furyl)-2-methylthieno[2,3-d]pyrimidin-4(3H)-one CAS 1082134-24-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1082134-24-4
Molecular FormulaC11H8N2O2S
Molecular Weight232.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(2-Furyl)-2-methylthieno[2,3-d]pyrimidin-4(3H)-one CAS 1082134-24-4 chemical structure

Description

5-(2-Furyl)-2-methylthieno[2,3-d]pyrimidin-4(3H)-one (CAS 1082134-24-4), molecular formula C11H8N2O2S and molecular weight 232.26 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 5-(2-Furyl)-2-methylthieno[2,3-d]pyrimidin-4(3H)-one (C11H8N2O2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), 5-(2-Furyl)-2-methylthieno[2,3-d]pyrimidin-4(3H)-one 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 FormulaC11H8N2O2S
Molecular Weight232.26 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms2
Sulfur Atoms1

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