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Home  > Chemistry  > Organic Building Blocks  > Sulfamides  > N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide

AE16386

1083326-75-3 | N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $75.00 $53.00 -   +
250mg 97% in stock $130.00 $91.00 -   +
1g 97% in stock $344.00 $241.00 -   +
5g 97% in stock $1,646.00 $1,153.00 -   +

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*All prices are in USD.

Description
Catalog Number: AE16386
Chemical Name: N-[2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-methanesulfonamide
CAS Number: 1083326-75-3
Molecular Formula: C13H21BN2O5S
Molecular Weight: 328.1922
MDL Number: MFCD12964555
SMILES: COc1ncc(cc1NS(=O)(=O)C)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 489  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • N-(2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)methanesulfonamide serves as a valuable building block in chemical synthesis due to its unique properties and reactivity. This compound is commonly used as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of C-C bonds under mild conditions. Its boron functionality allows for efficient incorporation into various organic structures, making it a versatile tool for the synthesis of complex molecules. Additionally, the methoxy and pyridine moieties provide additional structural diversity and potential for further derivatization, enhancing the compound's utility in the creation of diverse chemical libraries and pharmaceutical intermediates.
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