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Phenylboronic acid pinacol ester

ALDRICH/647098 - 97%

Synonym: (Pinacolboryl)benzene; 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane; Pinacol phenylboronate; cyclic tetramethylethylene ester benzeneboronic acid

CAS Number: 24388-23-6
Empirical Formula (Hill Notation): C12H17BO2
Molecular Weight: 204.07
MDL Number: MFCD00966985
Linear Formula: C12H17BO2
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-647098-5G 5 g
 $89.10
1/EA		 Add To Favorites
45-647098-10G 10 g
 $108.00
1/EA		 Add To Favorites
45-647098-50G 50 g
 $0.00
1/EA
CALL FOR PRICE		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 647098-50G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 647098-5G

 

assay 97%
form solid
InChI 1S/C12H17BO2/c1-11(2)12(3,4)15-13(14-11)10-8-6-5-7-9-10/h5-9H,1-4H3
InChI key KKLCYBZPQDOFQK-UHFFFAOYSA-N
mp 27-31 °C (lit.)
SMILES string CC1(C)OB(OC1(C)C)c2ccccc2
Application: Phenylboronic acid pinacol ester can be used:
• To prepare sulfinamide derivatives by reacting with diethylaminosulfur trifluoride (DAST) and potassium phenyltrifluoroborate.
• As a substrate in the study of Suzuki–Miyaura coupling of various aryl iodides over SiliaCat Pd(0).
General description: Phenylboronic acid, pinacol ester, also known as boronate ester, is generally used in metal-catalyzed C-C bond formation reactions like Suzuki–Miyaura reaction.
Packaging: 5, 10, 50 g in glass bottle
Purity 97%
mp 27-31 °C (lit.)
UNSPSC 12352103

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