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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 1-Acetyl-5,6-dihydro-2H-pyridine-4-boronic acid, pinacol ester

AA24445

1227068-67-8 | 1-Acetyl-5,6-dihydro-2H-pyridine-4-boronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $8.00 $6.00 -   +
250mg 98% in stock $10.00 $7.00 -   +
1g 98% in stock $21.00 $15.00 -   +
5g 98% in stock $101.00 $71.00 -   +
10g 98% in stock $194.00 $136.00 -   +
25g 98% in stock $482.00 $338.00 -   +

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Description
Catalog Number: AA24445
Chemical Name: 1-Acetyl-5,6-dihydro-2H-pyridine-4-boronic acid, pinacol ester
CAS Number: 1227068-67-8
Molecular Formula: C13H22BNO3
Molecular Weight: 251.1297
MDL Number: MFCD18427628
SMILES: CC(=O)N1CCC(=CC1)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 374  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route 
  • The compound 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2H)-yl)ethanone is utilized in chemical synthesis as a versatile building block. Its unique structure contains a boron atom, which can undergo various reactions to introduce functional groups into organic molecules. This compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where the boron moiety facilitates the coupling of two different organic fragments to form complex molecules. Additionally, the dihydropyridine ring system in the compound provides additional reactivity for further diversification of chemical structures. Overall, 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2H)-yl)ethanone serves as a key intermediate in the synthesis of advanced organic compounds with diverse applications.
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