![6-[(Pyridine-3-carbonyl)-amino]-hexanoic acid - chemical structure image](https://media.scbt.com/product/6--pyridine-3-carbonyl-amino-hexanoic-acid-structure_33_60_b_336084.jpg)
![6-[(Pyridine-3-carbonyl)-amino]-hexanoic acid - chemical structure image](https://media.scbt.com/product/6--pyridine-3-carbonyl-amino-hexanoic-acid-structure_33_60_t_336084.jpg "Molecular structure of 6-[(Pyridine-3-carbonyl)-amino]-hexanoic acid")
6-[(Pyridine-3-carbonyl)-amino]-hexanoic acid
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(E)-3-(tert-Butyldimethylsilyloxy)propene-1-yl-boronic acid pinacol ester functions as a reactant in organic synthesis. It acts as a reagent in the formation of carbon-carbon and carbon-heteroatom bonds, particularly in cross-coupling reactions. (E)-3-(Tert-Butyldimethylsilyloxy)Propene-1-Yl-Boronic Acid Pinacol Ester participates in Suzuki-Miyaura coupling reactions, where it undergoes transmetalation with a palladium catalyst to form a new carbon-carbon bond. The boronic acid pinacol ester moiety of the compound facilitates the transfer of the alkene group to the palladium catalyst, enabling the formation of the desired carbon-carbon bond. (E)-3-(Tert-Butyldimethylsilyloxy)Propene-1-Yl-Boronic Acid Pinacol Ester ′s mechanism of action involves its ability to undergo oxidative addition and reductive elimination processes, allowing it to participate in the construction of complex organic molecules.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
6-[(Pyridine-3-carbonyl)-amino]-hexanoic acid, 500 mg | sc-325731 | 500 mg | $248.00 |