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Home  > Boronic acid, B-[(1R)-3-methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(2-pyrazinylcarbonyl)amino]propyl]amino]butyl]-

AB02092

179324-69-7 | Boronic acid, B-[(1R)-3-methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(2-pyrazinylcarbonyl)amino]propyl]amino]butyl]-

Packsize Purity Availability Price Discounted Price    Quantity
1mg 95% in stock $42.00 $29.00 -   +
10mg 95% in stock $44.00 $31.00 -   +
100mg 95% in stock $120.00 $84.00 -   +
500mg 95% in stock $289.00 $202.00 -   +

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*All prices are in USD.

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Description
Catalog Number: AB02092
Chemical Name: Boronic acid, B-[(1R)-3-methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(2-pyrazinylcarbonyl)amino]propyl]amino]butyl]-
CAS Number: 179324-69-7
Molecular Formula: C19H25BN4O4
Molecular Weight: 384.2372
MDL Number: MFCD09056737
SMILES: CC(C[C@@H](B(O)O)NC(=O)[C@@H](NC(=O)c1cnccn1)Cc1ccccc1)C
NSC Number: 681239

 

Computed Properties
Complexity: 500  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 28  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 4  
Rotatable Bond Count: 9  

 

 

Upstream Synthesis Route 
  • The compound $name$ plays a crucial role in chemical synthesis as a versatile building block due to its unique structural features. It is specifically utilized as a boronic acid derivative for its ability to participate in various organic reactions and form stable covalent bonds with other molecules. In the realm of chemical synthesis, [(1R)-3-Methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(pyrazinylcarbonyl)amino]propyl]amino]butyl]boronic acid serves as a valuable reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of complex molecular structures through controlled and selective bond formations. Additionally, its chirality and functional groups make it a key component in the synthesis of pharmaceutical intermediates and other fine chemicals with high precision and efficiency.
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