2-(2-(4-Bromophenyl)-2-oxoethyl)isoindoline-1,3-dione CAS 794-43-4

Purity 97%+In StockPharmaceutical Standards
CAS No.794-43-4
Molecular FormulaC16H10BrNO3
Molecular Weight344.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2-(4-Bromophenyl)-2-oxoethyl)isoindoline-1,3-dione CAS 794-43-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 344.16 g/mol gives 2-(2-(4-Bromophenyl)-2-oxoethyl)isoindoline-1,3-dione distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-(2-(4-Bromophenyl)-2-oxoethyl)isoindoline-1,3-dione (CAS 794-43-4), a certified reference material (molecular formula C16H10BrNO3, MW 344.16 g/mol) for analytical method development and quality control.

Structurally, 2-(2-(4-Bromophenyl)-2-oxoethyl)isoindoline-1,3-dione (C16H10BrNO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 344.16 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-(4-Bromophenyl)-2-oxoethyl)isoindoline-1,3-dione 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 FormulaC16H10BrNO3
Molecular Weight344.16 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentBr-containing
Nitrogen Atoms1

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