(3-(1-(tert-Butoxy)-1-oxobutan-2-yl)phenyl)boronic acid CAS 2096341-60-3

Purity 97%+In StockPharmaceutical Standards
CAS No.2096341-60-3
Molecular FormulaC14H21BO4
Molecular Weight264.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-(1-(tert-Butoxy)-1-oxobutan-2-yl)phenyl)boronic acid CAS 2096341-60-3 chemical structure

Description

CATO manufactures (3-(1-(tert-Butoxy)-1-oxobutan-2-yl)phenyl)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.

(3-(1-(tert-Butoxy)-1-oxobutan-2-yl)phenyl)boronic acid (CAS 2096341-60-3) is a high-purity analytical reference standard with the molecular formula C14H21BO4 and a molecular weight of 264.13 g/mol.

Based on its molecular formula C14H21BO4, (3-(1-(tert-Butoxy)-1-oxobutan-2-yl)phenyl)boronic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 264.13 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC14H21BO4
Molecular Weight264.13 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997

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