3-(Ethoxycarbonyl)-2-methylphenylboronic Acid Pinacol Ester CAS 1198615-87-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1198615-87-0
Molecular FormulaC16H23BO4
Molecular Weight290.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(Ethoxycarbonyl)-2-methylphenylboronic Acid Pinacol Ester CAS 1198615-87-0 chemical structure

Description

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

3-(Ethoxycarbonyl)-2-methylphenylboronic Acid Pinacol Ester (CAS 1198615-87-0), molecular formula C16H23BO4 and molecular weight 290.16 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, 3-(Ethoxycarbonyl)-2-methylphenylboronic Acid Pinacol Ester is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 290.16 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 3-(Ethoxycarbonyl)-2-methylphenylboronic Acid Pinacol Ester 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 FormulaC16H23BO4
Molecular Weight290.16 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)5.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989

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Why CATO?