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CAS 877149-79-6

:

1-(2-chloroethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

Description:
1-(2-chloroethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a chemical compound characterized by its unique structure, which includes a pyrazole ring and a dioxaborolane moiety. The presence of the chloroethyl group suggests potential reactivity, particularly in nucleophilic substitution reactions. The dioxaborolane component is notable for its ability to participate in various chemical transformations, including cross-coupling reactions, making this compound of interest in synthetic organic chemistry. Its molecular structure indicates that it may exhibit specific physical properties such as solubility in organic solvents, and it may have applications in medicinal chemistry or material science due to the functional groups present. Additionally, the compound's stability and reactivity can be influenced by the steric hindrance provided by the tetramethyl groups, which may affect its interactions with biological targets or other reagents. Overall, this compound represents a versatile building block for further chemical synthesis and research applications.
Formula:C11H18BClN2O2
Synonyms:
  • 1-(2-chloroethyl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 1-(2-chloroethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 1H-Pyrazole, 1-(2-chloroethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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