2-(5-Bromo-2-oxochroman-4-yl)acetic acid CAS 1334499-95-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1334499-95-4
Molecular FormulaC11H9BrO4
Molecular Weight285.09 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(5-Bromo-2-oxochroman-4-yl)acetic acid CAS 1334499-95-4 chemical structure

Description

CATO supplies 2-(5-Bromo-2-oxochroman-4-yl)acetic acid (CAS 1334499-95-4), a certified reference material (molecular formula C11H9BrO4, MW 285.09 g/mol) for analytical method development and quality control.

The molecular framework of 2-(5-Bromo-2-oxochroman-4-yl)acetic acid (C11H9BrO4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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-(5-Bromo-2-oxochroman-4-yl)acetic acid 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 FormulaC11H9BrO4
Molecular Weight285.09 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentBr-containing

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