tert-Butyl 3-hydroxy-3-phenyl-8-azabicyclo[3.2.1]octane-8-carboxylate CAS 1307254-47-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1307254-47-2
Molecular FormulaC18H25NO3
Molecular Weight303.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 3-hydroxy-3-phenyl-8-azabicyclo[3.2.1]octane-8-carboxylate CAS 1307254-47-2 chemical structure

Description

The molecular framework of tert-Butyl 3-hydroxy-3-phenyl-8-azabicyclo[3.2.1]octane-8-carboxylate (C18H25NO3) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 3-hydroxy-3-phenyl-8-azabicyclo[3.2.1]octane-8-carboxylate (CAS 1307254-47-2), a certified reference material (molecular formula C18H25NO3, MW 303.40 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.

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 FormulaC18H25NO3
Molecular Weight303.40 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1

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