Tert-butyl 6-(benzyloxy)-1H-indole-1-carboxylate CAS 933474-39-6

Purity 97%+In StockPharmaceutical Standards
CAS No.933474-39-6
Molecular FormulaC20H21NO3
Molecular Weight323.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 6-(benzyloxy)-1H-indole-1-carboxylate CAS 933474-39-6 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Tert-butyl 6-(benzyloxy)-1H-indole-1-carboxylate.

CATO supplies Tert-butyl 6-(benzyloxy)-1H-indole-1-carboxylate (CAS 933474-39-6), a certified reference material (molecular formula C20H21NO3, MW 323.39 g/mol) for analytical method development and quality control.

Based on its molecular formula C20H21NO3, Tert-butyl 6-(benzyloxy)-1H-indole-1-carboxylate contains a steroid core, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 323.39 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.

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.

As a certified reference material (CRM), Tert-butyl 6-(benzyloxy)-1H-indole-1-carboxylate 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 FormulaC20H21NO3
Molecular Weight323.39 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

Recommended Standards

Why CATO?