Methyl 2-((5-methoxy-2-(3-(trifluoromethyl)phenyl)pyrimidin-4-yl)thio)acetate CAS 861209-10-1

Purity 97%+In StockPharmaceutical Standards
CAS No.861209-10-1
Molecular FormulaC15H13F3N2O3S
Molecular Weight358.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-((5-methoxy-2-(3-(trifluoromethyl)phenyl)pyrimidin-4-yl)thio)acetate CAS 861209-10-1 chemical structure

Description

Methyl 2-((5-methoxy-2-(3-(trifluoromethyl)phenyl)pyrimidin-4-yl)thio)acetate (CAS 861209-10-1) is a high-purity analytical reference standard with the molecular formula C15H13F3N2O3S and a molecular weight of 358.34 g/mol.

Structurally, Methyl 2-((5-methoxy-2-(3-(trifluoromethyl)phenyl)pyrimidin-4-yl)thio)acetate (C15H13F3N2O3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 358.34 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures Methyl 2-((5-methoxy-2-(3-(trifluoromethyl)phenyl)pyrimidin-4-yl)thio)acetate 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 FormulaC15H13F3N2O3S
Molecular Weight358.34 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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