tert-Butyl N-{[(5-chloro-2-methoxyphenyl)carbamoyl]methyl}carbamate CAS 1024396-69-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1024396-69-7
Molecular FormulaC14H19ClN2O4
Molecular Weight314.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl N-{[(5-chloro-2-methoxyphenyl)carbamoyl]methyl}carbamate CAS 1024396-69-7 chemical structure

Description

tert-Butyl N-{[(5-chloro-2-methoxyphenyl)carbamoyl]methyl}carbamate (CAS 1024396-69-7) is a high-purity analytical reference standard with the molecular formula C14H19ClN2O4 and a molecular weight of 314.76 g/mol.

The molecular framework of tert-Butyl N-{[(5-chloro-2-methoxyphenyl)carbamoyl]methyl}carbamate (C14H19ClN2O4) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 manufactures tert-Butyl N-{[(5-chloro-2-methoxyphenyl)carbamoyl]methyl}carbamate 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 FormulaC14H19ClN2O4
Molecular Weight314.76 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms2

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