(R)-tert-Butyl 3-((4-methylpyridin-2-yl)thio)pyrrolidine-1-carboxylate CAS 1354010-71-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1354010-71-1
Molecular FormulaC15H22N2O2S
Molecular Weight294.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-tert-Butyl 3-((4-methylpyridin-2-yl)thio)pyrrolidine-1-carboxylate CAS 1354010-71-1 chemical structure

Description

Based on its molecular formula C15H22N2O2S, (R)-tert-Butyl 3-((4-methylpyridin-2-yl)thio)pyrrolidine-1-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 294.41 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies (R)-tert-Butyl 3-((4-methylpyridin-2-yl)thio)pyrrolidine-1-carboxylate (CAS 1354010-71-1), a certified reference material (molecular formula C15H22N2O2S, MW 294.41 g/mol) for analytical method development and quality control.

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 (R)-tert-Butyl 3-((4-methylpyridin-2-yl)thio)pyrrolidine-1-carboxylate 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 FormulaC15H22N2O2S
Molecular Weight294.41 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.)1991
Nitrogen Atoms2
Sulfur Atoms1

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