tert-Butyl (S)-(1-Amino-3-phenyl-1-thioxopropan-2-yl)carbamate CAS 99281-95-5

Purity 97%+In StockPharmaceutical Standards
CAS No.99281-95-5
Molecular FormulaC14H20N2O2S
Molecular Weight280.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (S)-(1-Amino-3-phenyl-1-thioxopropan-2-yl)carbamate CAS 99281-95-5 chemical structure

Description

Based on its molecular formula C14H20N2O2S, tert-Butyl (S)-(1-Amino-3-phenyl-1-thioxopropan-2-yl)carbamate 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 280.39 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies tert-Butyl (S)-(1-Amino-3-phenyl-1-thioxopropan-2-yl)carbamate (CAS 99281-95-5), a certified reference material (molecular formula C14H20N2O2S, MW 280.39 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.

As a certified reference material (CRM), tert-Butyl (S)-(1-Amino-3-phenyl-1-thioxopropan-2-yl)carbamate 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 FormulaC14H20N2O2S
Molecular Weight280.39 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.)1985
Nitrogen Atoms2
Sulfur Atoms1

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