tert-Butyl (2-bromo-4-fluoro-6-iodophenyl)carbamate CAS 1447607-24-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1447607-24-0
Molecular FormulaC11H12BrFINO2
Molecular Weight416.03 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (2-bromo-4-fluoro-6-iodophenyl)carbamate CAS 1447607-24-0 chemical structure

Description

CATO supplies tert-Butyl (2-bromo-4-fluoro-6-iodophenyl)carbamate (CAS 1447607-24-0), a certified reference material (molecular formula C11H12BrFINO2, MW 416.03 g/mol) for analytical method development and quality control.

tert-Butyl (2-bromo-4-fluoro-6-iodophenyl)carbamate (C11H12BrFINO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/bromine/iodine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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-bromo-4-fluoro-6-iodophenyl)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 FormulaC11H12BrFINO2
Molecular Weight416.03 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, 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.)1992
Halogen ContentF/Br/I-containing
Nitrogen Atoms1

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