5-Bromo-2-chlorobicyclo[4.2.0]Octa-1,3,5-triene-7-carboxylic acid CAS 1135490-73-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1135490-73-1
Molecular FormulaC9H6BrClO2
Molecular Weight261.50 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Bromo-2-chlorobicyclo[4.2.0]Octa-1,3,5-triene-7-carboxylic acid CAS 1135490-73-1 chemical structure

Description

CATO supplies 5-Bromo-2-chlorobicyclo[4.2.0]Octa-1,3,5-triene-7-carboxylic acid (CAS 1135490-73-1), a certified reference material (molecular formula C9H6BrClO2, MW 261.50 g/mol) for analytical method development and quality control.

5-Bromo-2-chlorobicyclo[4.2.0]Octa-1,3,5-triene-7-carboxylic acid (C9H6BrClO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/bromine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 5-Bromo-2-chlorobicyclo[4.2.0]Octa-1,3,5-triene-7-carboxylic 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 FormulaC9H6BrClO2
Molecular Weight261.50 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl/Br-containing

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