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(4-Methylphenyl)cyclic-triolborate Potassium Salt

for Organic Synthesis
Manufacturer :
FUJIFILM Wako Pure Chemical Corporation
Storage Condition :
Keep at 2-10 degrees C.
Molecular Formula :
C12H16BKO3
Molecular Weight :
258.16
  • Structural Formula
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Distributor
134-16061
Barcode No
4987481488076
1G
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Distributor
130-16063
Barcode No
4987481488083
5G
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Document

Product Specification Sheet
Package Insert
Certificate of Analysis
Calibration Certificate
Analytical Charts

Overview / Applications

Outline Green Chemistry

This product is for research use only. Do not administer it to human.

Suzuki-Miyaura coupling reaction is carried out typically in the presence of a base and often in the coexistence of water as many boronic acids convert to cyclic anhydrides by dehydrotrimerization. However, since some boronic acids are hydrolyzed in basic aqueous solution, a large excess of boronic acids are often required.
Organic cyclic-triolborate salts are the ate complexed borate reagents developed by Miyaura, et al.
There is no need to add bases in cross coupling reactions catalyzed by palladium. They may be used in aqueous and nonaqueous systems. They are also useful in N-arylation reaction with copper catalysts.

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Precautions for Use Packed on inactive gas

Property

Appearance White - slightly yellowish brown, crystals - powder or mass

Manufacturer Information

Alias

  • [2-(Hydroxymethyl)-2-methyl-1,3-propanediolato-O,O',O''](4-methylphenyl)borate Potassium Salt
    Active Boronic Acid

For research use or further manufacturing use only. Not for use in diagnostic procedures.

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