Ethyl 4-iodo-2-(methylthio)pyrimidine-5-carboxylate CAS 1133-91-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1133-91-1
Molecular FormulaC8H9IN2O2S
Molecular Weight324.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 4-iodo-2-(methylthio)pyrimidine-5-carboxylate CAS 1133-91-1 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

CATO supplies Ethyl 4-iodo-2-(methylthio)pyrimidine-5-carboxylate (CAS 1133-91-1), a certified reference material (molecular formula C8H9IN2O2S, MW 324.14 g/mol) for analytical method development and quality control.

Ethyl 4-iodo-2-(methylthio)pyrimidine-5-carboxylate (C8H9IN2O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; 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 FormulaC8H9IN2O2S
Molecular Weight324.14 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentI-containing
Nitrogen Atoms2
Sulfur Atoms1

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