Tert-butyl (1S,6R)-8-((R)-1-phenylethyl)-3,8-diazabicyclo[4.2.0]Octane-3-carboxylate CAS 923956-64-3

Purity 97%+In StockPharmaceutical Standards
CAS No.923956-64-3
Molecular FormulaC19H28N2O2
Molecular Weight316.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl (1S,6R)-8-((R)-1-phenylethyl)-3,8-diazabicyclo[4.2.0]Octane-3-carboxylate CAS 923956-64-3 chemical structure

Description

CATO supplies Tert-butyl (1S,6R)-8-((R)-1-phenylethyl)-3,8-diazabicyclo[4.2.0]Octane-3-carboxylate (CAS 923956-64-3), a certified reference material (molecular formula C19H28N2O2, MW 316.44 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, Tert-butyl (1S,6R)-8-((R)-1-phenylethyl)-3,8-diazabicyclo[4.2.0]Octane-3-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 316.44 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

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.

Physical & Chemical Properties

Molecular FormulaC19H28N2O2
Molecular Weight316.44 g/mol
AppearanceOff-white to pale yellow crystalline powder
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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