[(2-Chlorophenyl)methyl]boronic acid CAS 1350512-46-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1350512-46-7
Molecular FormulaC7H8BClO2
Molecular Weight170.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[(2-Chlorophenyl)methyl]boronic acid CAS 1350512-46-7 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 [(2-Chlorophenyl)methyl]boronic acid.

CATO supplies [(2-Chlorophenyl)methyl]boronic acid (CAS 1350512-46-7), a certified reference material (molecular formula C7H8BClO2, MW 170.40 g/mol) for analytical method development and quality control.

[(2-Chlorophenyl)methyl]boronic acid (C7H8BClO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. 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. 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-Chlorophenyl)methyl]boronic 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 FormulaC7H8BClO2
Molecular Weight170.40 g/mol
Purity97%+
StorageStore at 2-8°C, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.5
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1991
Halogen ContentCl-containing

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