2-(Chloromethyl)-5-(4-chlorophenyl)-3h,4h-thieno[2,3-d]pyrimidin-4-one CAS 91225-69-3

Purity 97%+In StockPharmaceutical Standards
CAS No.91225-69-3
Molecular FormulaC13H8Cl2N2OS
Molecular Weight311.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Chloromethyl)-5-(4-chlorophenyl)-3h,4h-thieno[2,3-d]pyrimidin-4-one CAS 91225-69-3 chemical structure

Description

CATO manufactures 2-(Chloromethyl)-5-(4-chlorophenyl)-3h,4h-thieno[2,3-d]pyrimidin-4-one 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.

2-(Chloromethyl)-5-(4-chlorophenyl)-3h,4h-thieno[2,3-d]pyrimidin-4-one (CAS 91225-69-3) is a high-purity analytical reference standard with the molecular formula C13H8Cl2N2OS and a molecular weight of 311.19 g/mol.

2-(Chloromethyl)-5-(4-chlorophenyl)-3h,4h-thieno[2,3-d]pyrimidin-4-one (C13H8Cl2N2OS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

Physical & Chemical Properties

Molecular FormulaC13H8Cl2N2OS
Molecular Weight311.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1983
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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