logo
Home  > Chemistry  > Organometallic Reagents  > Organoboron  > 1-Boc-3,5-dimethylpyrazole-4-boronic acid pinacol ester

AB79352

1073354-70-7 | 1-Boc-3,5-dimethylpyrazole-4-boronic acid pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $23.00 $16.00 -   +
200mg 97% in stock $36.00 $25.00 -   +
250mg 97% in stock $38.00 $27.00 -   +
1g 97% in stock $60.00 $42.00 -   +
5g 97% in stock $231.00 $162.00 -   +

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

*All prices are in USD.

Request Bulk Quote
Description
Catalog Number: AB79352
Chemical Name: 1-Boc-3,5-dimethylpyrazole-4-boronic acid pinacol ester
CAS Number: 1073354-70-7
Molecular Formula: C16H27BN2O4
Molecular Weight: 322.2076
MDL Number: MFCD09027070
SMILES: Cc1nn(c(c1B1OC(C(O1)(C)C)(C)C)C)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 459  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 23  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route 
  • The tert-Butyl 3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate is a versatile compound that finds valuable applications in chemical synthesis. As a key building block in organic chemistry, this compound is commonly used as a reagent in various chemical reactions to introduce the tert-butyl ester functionality and the pyrazole ring structure simultaneously. Its unique molecular structure facilitates the formation of complex molecules with high efficiency and selectivity, making it a preferred choice in the synthesis of pharmaceuticals, agrochemicals, and materials science. Furthermore, the presence of the boron-diol moiety in this compound enables it to participate in diverse transformations such as Suzuki-Miyaura cross-coupling reactions, offering synthetic chemists a powerful tool for the construction of C-C bonds.
FEATURED PRODUCTS