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Home  > Chemistry  > Organic Building Blocks  > Amides  > (4-(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)phenyl)boronic acid pinacol ester

AI12028

1187313-16-1 | (4-(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)phenyl)boronic acid pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $153.00 $107.00 -   +
250mg 98% in stock $249.00 $175.00 -   +
1g 98% in stock $556.00 $390.00 -   +
5g 98% in stock $1,878.00 $1,315.00 -   +
10g 98% in stock $2,810.00 $1,967.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI12028
Chemical Name: (4-(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)phenyl)boronic acid pinacol ester
CAS Number: 1187313-16-1
Molecular Formula: C22H32BNO4
Molecular Weight: 385.3048
MDL Number: MFCD28403579
SMILES: O=C(N1CCC(=CC1)c1ccc(cc1)B1OC(C(O1)(C)C)(C)C)OC(C)(C)C

 

Computed Properties
Complexity: 599  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 28  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • The (4-(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)phenyl)boronic acid pinacol ester, hereafter referred to as $name$, is a highly valuable compound in chemical synthesis, particularly in the field of organic chemistry. This compound is widely utilized as a versatile building block in the creation of complex molecular structures.$name$ serves as a critical reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of C-C bonds between aryl or vinyl boronic acids and various organic electrophiles. The presence of the boronic acid functionality in $name$ allows for selective and efficient coupling reactions, making it an essential tool for constructing diverse molecular architectures.Moreover, $name$ plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its ability to facilitate the introduction of functional groups with high regio- and stereo-selectivity makes it a preferred choice for chemists working on the development of novel bioactive compounds and advanced materials.In summary, the application of $name$ in chemical synthesis extends beyond mere reactions; it represents a fundamental building block that enables chemists to access a wide range of complex molecules with precision and efficiency.
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