tert-Butyl 3-(2-(4-chlorophenyl)acetyl)benzylcarbamate CAS 1017781-63-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1017781-63-3
Molecular FormulaC20H22ClNO3
Molecular Weight359.85 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 3-(2-(4-chlorophenyl)acetyl)benzylcarbamate CAS 1017781-63-3 chemical structure

Description

CATO manufactures tert-Butyl 3-(2-(4-chlorophenyl)acetyl)benzylcarbamate 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.

tert-Butyl 3-(2-(4-chlorophenyl)acetyl)benzylcarbamate (CAS 1017781-63-3), molecular formula C20H22ClNO3 and molecular weight 359.85 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, tert-Butyl 3-(2-(4-chlorophenyl)acetyl)benzylcarbamate (C20H22ClNO3) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 359.85 g/mol, it falls into the moderately-high-molecular-weight range. 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.

Physical & Chemical Properties

Molecular FormulaC20H22ClNO3
Molecular Weight359.85 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms1

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