tert-Butyl 4-phenyl-2,3,4,5-tetrahydro-1h-1,5-benzodiazepine-1-carboxylate CAS 904815-39-0

Purity 97%+In StockPharmaceutical Standards
CAS No.904815-39-0
Molecular FormulaC20H24N2O2
Molecular Weight324.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 4-phenyl-2,3,4,5-tetrahydro-1h-1,5-benzodiazepine-1-carboxylate CAS 904815-39-0 chemical structure

Description

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO supplies tert-Butyl 4-phenyl-2,3,4,5-tetrahydro-1h-1,5-benzodiazepine-1-carboxylate (CAS 904815-39-0), a certified reference material (molecular formula C20H24N2O2, MW 324.42 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 4-phenyl-2,3,4,5-tetrahydro-1h-1,5-benzodiazepine-1-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 324.42 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.

CATO manufactures tert-Butyl 4-phenyl-2,3,4,5-tetrahydro-1h-1,5-benzodiazepine-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 FormulaC20H24N2O2
Molecular Weight324.42 g/mol
AppearancePale yellow to 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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