2-(2-((5-(4-Chlorophenyl)thieno[2,3-d]pyrimidin-4-yl)amino)ethoxy)ethan-1-ol CAS 457919-69-6

Purity 97%+In StockPharmaceutical Standards
CAS No.457919-69-6
Molecular FormulaC16H16ClN3O2S
Molecular Weight349.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2-((5-(4-Chlorophenyl)thieno[2,3-d]pyrimidin-4-yl)amino)ethoxy)ethan-1-ol CAS 457919-69-6 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 2-(2-((5-(4-Chlorophenyl)thieno[2,3-d]pyrimidin-4-yl)amino)ethoxy)ethan-1-ol (CAS 457919-69-6), a certified reference material (molecular formula C16H16ClN3O2S, MW 349.84 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H16ClN3O2S, 2-(2-((5-(4-Chlorophenyl)thieno[2,3-d]pyrimidin-4-yl)amino)ethoxy)ethan-1-ol contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 349.84 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 2-(2-((5-(4-Chlorophenyl)thieno[2,3-d]pyrimidin-4-yl)amino)ethoxy)ethan-1-ol 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 FormulaC16H16ClN3O2S
Molecular Weight349.84 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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