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2-Phenylethylboronic acid pinacol ester
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2-Phenylethylboronic acid pinacol ester

CAS: 165904-22-3

Ref. 3D-FP162033

1gDiscontinued
2gDiscontinued
5gDiscontinued
10gDiscontinued
25gDiscontinued

Discontinued product. For inquiries about similar products, please fill out our form or email us at .


Product Information

Name:
2-Phenylethylboronic acid pinacol ester
Synonyms:
  • 4,4,5,5-Tetramethyl-2-(2-Phenylethyl)-1,3,2-Dioxaborolane
Description:

2-Phenylethylboronic acid pinacol ester is an aliphatic boronic acid that can be used in the stereoselective synthesis of 1,2-dienes. It is a reactive intermediate that has been shown to undergo a spontaneous cyclization reaction with a variety of olefins to form cyclohexadienes. The regioselectivity of these reactions can be controlled by varying the reaction conditions, such as temperature, solvent, and pressure. This reactivity was shown using chloride as an impurity, which acts both as a competitive inhibitor and an activator for the reaction. Furthermore, this reactivity has been studied using iron oxide nanoparticles (IONPs) as a catalyst which led to higher yields and more control over the product distribution.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
232.13 g/mol
Formula:
C14H21BO2
Purity:
Min. 95%
InChI:
InChI=1S/C14H21BO2/c1-13(2)14(3,4)17-15(16-13)11-10-12-8-6-5-7-9-12/h5-9H,10-11H2,1-4H3
InChI key:
InChIKey=LVLQNRWCBBIVHR-UHFFFAOYSA-N
SMILES:
CC1(C)OB(CCc2ccccc2)OC1(C)C
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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