Benzylboronic acid pinacol ester, 96%
Benzylboronic acid pinacol ester, 96%
Benzylboronic acid pinacol ester, 96%
Benzylboronic acid pinacol ester, 96%
Thermo Scientific Chemicals

Benzylboronic acid pinacol ester, 96%

CAS: 87100-28-5 | C13H19BO2 | 218.103 g/mol
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1 g
5 g
25 g
Catalog number H32523.14
also known as H32523-14
Price (EUR)
545,00
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Quantity:
25 g
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Price (EUR)
545,00
Each
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Chemical Identifiers
CAS87100-28-5
IUPAC Name2-benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Molecular FormulaC13H19BO2
InChI KeyYCNQPAVKQPLZRS-UHFFFAOYSA-N
SMILESCC1(C)OB(CC2=CC=CC=C2)OC1(C)C
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear to faintly turbid colorless to pale yellow
FormLiquid
Assay (GC)≥95.0%
Refractive Index1.4850-1.4910 @ 20?C
Benzylboronic acid pinacol ester finds application in Pd (0)-mediated [11 C] carbonylation reaction.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Benzylboronic acid pinacol ester finds application in Pd (0)-mediated [11 C] carbonylation reaction.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Shunsuke Sueki,; Yoichiro Kuninobu. Copper-Catalyzed N- and O-Alkylation of Amines and Phenols using Alkylborane Reagents. Org. Lett. 2013, 15(7),1544-1547.
  2. Hideki Ishii,; Katsuyuki Minegishi,; Koutaro Nagatsu,; Ming-Rong Zhang. Pd(0)-mediated [11C]carbonylation of aryl and heteroaryl boronic acid pinacol esters with [11C]carbon monoxide under ambient conditions and a facile process for the conversion of [carbonyl-11C]esters to [carbonyl-11C]amides. Tetrahedron. 2015, 71 (10),1588-1596.