Tert-butyl (3-bromo-5-chloro-2-methoxyphenyl)carbamate CAS 1485204-67-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1485204-67-8
Molecular FormulaC12H15BrClNO3
Molecular Weight336.61 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl (3-bromo-5-chloro-2-methoxyphenyl)carbamate CAS 1485204-67-8 chemical structure

Description

CATO supplies Tert-butyl (3-bromo-5-chloro-2-methoxyphenyl)carbamate (CAS 1485204-67-8), a certified reference material (molecular formula C12H15BrClNO3, MW 336.61 g/mol) for analytical method development and quality control.

The molecular framework of Tert-butyl (3-bromo-5-chloro-2-methoxyphenyl)carbamate (C12H15BrClNO3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/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. 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.

CATO manufactures Tert-butyl (3-bromo-5-chloro-2-methoxyphenyl)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 FormulaC12H15BrClNO3
Molecular Weight336.61 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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; Hygroscopic; reseal immediately after opening; 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 ContentCl/Br-containing
Nitrogen Atoms1

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