tert-Butyl (5-bromo-2-fluoro-3-(trifluoromethyl)phenyl)carbamate CAS 2287287-41-4

Purity 97%+In StockPharmaceutical Standards
CAS No.2287287-41-4
Molecular FormulaC12H12BrF4NO2
Molecular Weight358.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (5-bromo-2-fluoro-3-(trifluoromethyl)phenyl)carbamate CAS 2287287-41-4 chemical structure

Description

CATO supplies tert-Butyl (5-bromo-2-fluoro-3-(trifluoromethyl)phenyl)carbamate (CAS 2287287-41-4), a certified reference material (molecular formula C12H12BrF4NO2, MW 358.13 g/mol) for analytical method development and quality control.

The molecular framework of tert-Butyl (5-bromo-2-fluoro-3-(trifluoromethyl)phenyl)carbamate (C12H12BrF4NO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/bromine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 (5-bromo-2-fluoro-3-(trifluoromethyl)phenyl)carbamate 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 FormulaC12H12BrF4NO2
Molecular Weight358.13 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Halogen ContentF/Br-containing
Nitrogen Atoms1

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