tert-Butyl 2-benzylisoindoline-1-carboxylate CAS 84385-22-8

Purity 97%+In StockPharmaceutical Standards
CAS No.84385-22-8
Molecular FormulaC20H23NO2
Molecular Weight309.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 2-benzylisoindoline-1-carboxylate CAS 84385-22-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 309.40 g/mol gives tert-Butyl 2-benzylisoindoline-1-carboxylate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

tert-Butyl 2-benzylisoindoline-1-carboxylate (CAS 84385-22-8), molecular formula C20H23NO2 and molecular weight 309.40 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C20H23NO2, tert-Butyl 2-benzylisoindoline-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 309.40 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 2-benzylisoindoline-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 FormulaC20H23NO2
Molecular Weight309.40 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1981
Nitrogen Atoms1

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