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Isopropylboronic acid pinacol ester, 97%, Thermo Scientific Chemicals
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Catalog number H33861.03
also known as H33861-03
Price (EUR)/ Each
21,89
Online exclusive
24.60 Save 2,71 (11%)
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Quantity:
1 g
Price (EUR)/ Each
21,89
Online exclusive
24.60 Save 2,71 (11%)
Isopropylboronic acid pinacol ester, 97%, Thermo Scientific Chemicals
Catalog numberH33861.03
Price (EUR)/ Each
21,89
Online exclusive
24.60 Save 2,71 (11%)
-
Chemical Identifiers
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
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Specifications
Specification Sheet
Specification SheetFormLiquid
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.
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:
- 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.
- 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.