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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyrimidines  > 2-(tert-Butoxycarbonylamino)pyrimidine-5-boronic acid, pinacol ester

AD80705

1032758-88-5 | 2-(tert-Butoxycarbonylamino)pyrimidine-5-boronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $66.00 $46.00 -   +
250mg 98% in stock $99.00 $69.00 -   +
1g 98% in stock $215.00 $150.00 -   +
5g 98% in stock $750.00 $525.00 -   +
25g 98% in stock $3,089.00 $2,162.00 -   +

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*All prices are in USD.

Description
Catalog Number: AD80705
Chemical Name: 2-(tert-Butoxycarbonylamino)pyrimidine-5-boronic acid, pinacol ester
CAS Number: 1032758-88-5
Molecular Formula: C15H24BN3O4
Molecular Weight: 321.1798
MDL Number: MFCD09027069
SMILES: O=C(OC(C)(C)C)Nc1ncc(cn1)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 427  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 23  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • The tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-yl)carbamate is a versatile compound used in chemical synthesis for its unique reactivity and selectivity. It serves as a valuable reagent in various organic transformations, particularly in cross-coupling reactions and palladium-catalyzed coupling reactions.This compound is commonly employed as a protecting group for amines due to its stability under various reaction conditions. It allows for the selective modification of molecules by masking the amine functionality and enabling specific transformations to occur at other reactive sites. Additionally, the presence of the boronate ester moiety in the molecule enhances its utility in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of C-C bonds in a controlled manner.Moreover, the tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-yl)carbamate exhibits excellent solubility in common organic solvents, making it convenient for use in various synthetic protocols. Its compatibility with a wide range of reaction conditions and functional groups further enhances its value as a strategic building block for complex molecule synthesis in medicinal chemistry and material science.
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