Methyl 4-cyclopropyl-2-(methylthio)pyrimidine-5-carboxylate CAS 1072944-76-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1072944-76-3
Molecular FormulaC10H12N2O2S
Molecular Weight224.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-cyclopropyl-2-(methylthio)pyrimidine-5-carboxylate CAS 1072944-76-3 chemical structure

Description

Methyl 4-cyclopropyl-2-(methylthio)pyrimidine-5-carboxylate (C10H12N2O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

Methyl 4-cyclopropyl-2-(methylthio)pyrimidine-5-carboxylate (CAS 1072944-76-3) is a high-purity analytical reference standard with the molecular formula C10H12N2O2S and a molecular weight of 224.28 g/mol.

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), Methyl 4-cyclopropyl-2-(methylthio)pyrimidine-5-carboxylate 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 FormulaC10H12N2O2S
Molecular Weight224.28 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2
Sulfur Atoms1

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