2-Bromo-4-isopropoxy-5-methoxybenzoyl chloride CAS 1160250-46-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1160250-46-3
Molecular FormulaC11H12BrClO3
Molecular Weight307.57 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Bromo-4-isopropoxy-5-methoxybenzoyl chloride CAS 1160250-46-3 chemical structure

Description

Based on its molecular formula C11H12BrClO3, 2-Bromo-4-isopropoxy-5-methoxybenzoyl chloride contains a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/bromine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 307.57 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 2-Bromo-4-isopropoxy-5-methoxybenzoyl chloride (CAS 1160250-46-3), a certified reference material (molecular formula C11H12BrClO3, MW 307.57 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 2-Bromo-4-isopropoxy-5-methoxybenzoyl chloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H12BrClO3
Molecular Weight307.57 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; 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.)1989
Halogen ContentCl/Br-containing

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