2-[(2-Bromo-4-nitrophenyl)sulfanyl]-1,3-dichlorobenzene CAS 477888-99-6

Purity 97%+In StockPharmaceutical Standards
CAS No.477888-99-6
Molecular FormulaC12H6BrCl2NO2S
Molecular Weight379.06 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[(2-Bromo-4-nitrophenyl)sulfanyl]-1,3-dichlorobenzene CAS 477888-99-6 chemical structure

Description

2-[(2-Bromo-4-nitrophenyl)sulfanyl]-1,3-dichlorobenzene (CAS 477888-99-6), molecular formula C12H6BrCl2NO2S and molecular weight 379.06 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 2-[(2-Bromo-4-nitrophenyl)sulfanyl]-1,3-dichlorobenzene (C12H6BrCl2NO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone 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. 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.

CATO manufactures 2-[(2-Bromo-4-nitrophenyl)sulfanyl]-1,3-dichlorobenzene 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 FormulaC12H6BrCl2NO2S
Molecular Weight379.06 g/mol
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl/Br-containing
Nitrogen Atoms1
Sulfur Atoms1

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