2-(Chloromethyl)-5-(5-methylthiophen-2-yl)-3h,4h-thieno[2,3-d]pyrimidin-4-one CAS 851116-05-7

Purity 97%+In StockPharmaceutical Standards
CAS No.851116-05-7
Molecular FormulaC12H9ClN2OS2
Molecular Weight296.80 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Chloromethyl)-5-(5-methylthiophen-2-yl)-3h,4h-thieno[2,3-d]pyrimidin-4-one CAS 851116-05-7 chemical structure

Description

CATO supplies 2-(Chloromethyl)-5-(5-methylthiophen-2-yl)-3h,4h-thieno[2,3-d]pyrimidin-4-one (CAS 851116-05-7), a certified reference material (molecular formula C12H9ClN2OS2, MW 296.80 g/mol) for analytical method development and quality control.

The molecular framework of 2-(Chloromethyl)-5-(5-methylthiophen-2-yl)-3h,4h-thieno[2,3-d]pyrimidin-4-one (C12H9ClN2OS2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution. 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. 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.

As a certified reference material (CRM), 2-(Chloromethyl)-5-(5-methylthiophen-2-yl)-3h,4h-thieno[2,3-d]pyrimidin-4-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 FormulaC12H9ClN2OS2
Molecular Weight296.80 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms2

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