tert-Butyl 3-((4-cyanophenyl)sulfonyl)pyrrolidine-1-carboxylate CAS 887587-78-2

Purity 97%+In StockPharmaceutical Standards
CAS No.887587-78-2
Molecular FormulaC16H20N2O4S
Molecular Weight336.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 3-((4-cyanophenyl)sulfonyl)pyrrolidine-1-carboxylate CAS 887587-78-2 chemical structure

Description

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

tert-Butyl 3-((4-cyanophenyl)sulfonyl)pyrrolidine-1-carboxylate (CAS 887587-78-2), molecular formula C16H20N2O4S and molecular weight 336.41 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C16H20N2O4S, tert-Butyl 3-((4-cyanophenyl)sulfonyl)pyrrolidine-1-carboxylate contains a flavonoid core, 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 336.41 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

CATO manufactures tert-Butyl 3-((4-cyanophenyl)sulfonyl)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 FormulaC16H20N2O4S
Molecular Weight336.41 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2
Sulfur Atoms1

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