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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyrazoles  > Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazol-1-yl)propanoate

AA55178

1220968-24-0 | Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazol-1-yl)propanoate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $8.00 $6.00 -   +
250mg 95% in stock $19.00 $14.00 -   +
5g 95% in stock $320.00 $224.00 -   +
10g 95% in stock $614.00 $430.00 -   +
25g 95% in stock $1,516.00 $1,061.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA55178
Chemical Name: Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazol-1-yl)propanoate
CAS Number: 1220968-24-0
Molecular Formula: C14H23BN2O4
Molecular Weight: 294.1544
MDL Number: MFCD27996757
SMILES: CCOC(=O)C(n1ncc(c1)B1OC(C(O1)(C)C)(C)C)C

 

Computed Properties
Complexity: 386  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propanoate is a valuable compound used in chemical synthesis for its unique properties and versatile applications. It serves as a key building block in organic chemistry reactions, particularly in the formation of complex molecules with pharmaceutical, agrochemical, and material science applications.This compound can act as a functionalized reagent in various transformations, enabling the introduction of the pyrazole moiety into target molecules. Its boron-containing group offers opportunities for further modification through metal-catalyzed cross-coupling reactions, making it a valuable tool in the synthesis of biologically active compounds and advanced materials.With its specific structural features, Ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propanoate provides chemists with a powerful means to access complex molecular architectures efficiently and selectively. Its utility extends to the creation of molecular probes, ligands, and drug candidates, highlighting its significance in modern chemical research and development.
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