4-Methoxy-3-(1-methylethyl)phenylboronic acid pinacol ester CAS 2121513-08-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2121513-08-2
Molecular FormulaC16H25BO3
Molecular Weight276.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Methoxy-3-(1-methylethyl)phenylboronic acid pinacol ester CAS 2121513-08-2 chemical structure

Description

As a certified reference material (CRM), 4-Methoxy-3-(1-methylethyl)phenylboronic acid pinacol ester 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.

4-Methoxy-3-(1-methylethyl)phenylboronic acid pinacol ester (CAS 2121513-08-2) is a high-purity analytical reference standard with the molecular formula C16H25BO3 and a molecular weight of 276.18 g/mol.

4-Methoxy-3-(1-methylethyl)phenylboronic acid pinacol ester (C16H25BO3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility, 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.

Physical & Chemical Properties

Molecular FormulaC16H25BO3
Molecular Weight276.18 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997

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