CymitQuimica logo

CAS 947249-41-4

:

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine

Description:
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine is a chemical compound characterized by its unique structure, which includes a pyrazin-2-amine moiety and a boron-containing dioxaborolane group. This compound typically exhibits properties associated with both amines and boron compounds, such as potential reactivity in nucleophilic substitution reactions and the ability to form coordination complexes. The presence of the dioxaborolane group suggests that it may participate in reactions involving boron, such as Suzuki coupling, which is significant in organic synthesis. Additionally, the tetramethyl substitution enhances its stability and solubility in organic solvents. The compound may also exhibit biological activity, making it of interest in medicinal chemistry. Its specific applications can vary, but it is often explored in the context of drug development and materials science due to its functional groups. As with any chemical substance, safety data and handling precautions should be observed, particularly regarding its reactivity and potential toxicity.
Formula:C10H16BN3O2
InChI:InChI=1S/C10H16BN3O2/c1-9(2)10(3,4)16-11(15-9)7-5-14-8(12)6-13-7/h5-6H,1-4H3,(H2,12,14)
InChI key:InChIKey=CBNIRWXQQRNRJY-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=NC(N)=CN2
Synonyms:
  • 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyrazinamine
  • 2-Pyrazinamine, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine
  • (5-Aminopyrazin-2-yl)boronic acid pinacol ester
  • 2-(5-Aminopyrazin-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.