3-(4-Bromophenyl)-2-tosylacrylonitrile CAS 811826-58-1

Purity 97%+In StockPharmaceutical Standards
CAS No.811826-58-1
Molecular FormulaC16H12BrNO2S
Molecular Weight362.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Bromophenyl)-2-tosylacrylonitrile CAS 811826-58-1 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-(4-Bromophenyl)-2-tosylacrylonitrile.

3-(4-Bromophenyl)-2-tosylacrylonitrile (CAS 811826-58-1) is a high-purity analytical reference standard with the molecular formula C16H12BrNO2S and a molecular weight of 362.24 g/mol.

The molecular framework of 3-(4-Bromophenyl)-2-tosylacrylonitrile (C16H12BrNO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, 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 3-(4-Bromophenyl)-2-tosylacrylonitrile 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 FormulaC16H12BrNO2S
Molecular Weight362.24 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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