Isopropylboronic acid pinacol ester, 97%
Isopropylboronic acid pinacol ester, 97%
Isopropylboronic acid pinacol ester, 97%
Thermo Scientific Chemicals

Isopropylboronic acid pinacol ester, 97%

CAS: 76347-13-2 | C9H19BO2 | 170.059 g/mol
製品番号(カタログ番号) H33861.03
または、製品番号H33861-03
価格(JPY)
-
数量:
1 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS76347-13-2
IUPAC Name4,4,5,5-tetramethyl-2-(propan-2-yl)-1,3,2-dioxaborolane
Molecular FormulaC9H19BO2
InChI KeyMECCSFDHAVAAAW-UHFFFAOYSA-N
SMILESCC(C)B1OC(C)(C)C(C)(C)O1
さらに表示
FormLiquid
Refractive Index1.4070-1.4110 @ 20°C
Appearance (Color)Clear colorless
Assay (GC)≥96.0%
Isopropylboronic acid pinacol ester is used as pharmaceutical intermediate.

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
Isopropylboronic acid pinacol ester is used as pharmaceutical intermediate.

Solubility
Slightly soluble in water.

Notes
Store in a cool, dry place, in a well sealed container. Store away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Tim G. Elford; Stefan Nave; Ravindra P. Sonawane and Varinder K. Aggarwal. Total Synthesis of (+)-Erogorgiaene Using Lithiation-Borylation Methodology, and Stereoselective Synthesis of Each of Its Diastereoisomers. J. Am. Chem. Soc. 2011, 133 (42), 16798-16801.
  2. Dr. Benjamin M. Partridge; Dr. Laëtitia Chausset-Boissarie; Matthew Burns; Alexander P. Pulis; Prof. Varinder K. Aggarwal. Enantioselective Synthesis and Cross-Coupling of Tertiary Propargylic Boronic Esters Using Lithiation-Borylation of Propargylic Carbamates. Angewandte Chemie International Edition. 2010, 51 (47), 11795-11799.