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CAS 138900-55-7

:

[1-[tris(1-Methylethyl)silyl]-1H-pyrrol-3-yl]-boronic acid

Description:
[1-[tris(1-Methylethyl)silyl]-1H-pyrrol-3-yl]-boronic acid, with the CAS number 138900-55-7, is a boronic acid derivative characterized by the presence of a pyrrole ring substituted with a tris(1-methylethyl)silyl group. This compound typically exhibits properties associated with both boronic acids and organosilicon compounds, including the ability to form reversible covalent bonds with diols, which is significant for applications in organic synthesis and materials science. The presence of the silyl group enhances its stability and solubility in organic solvents, making it useful in various chemical reactions, including cross-coupling reactions. Additionally, boronic acids are known for their role in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. The compound's unique structure may also impart specific reactivity patterns, making it a valuable intermediate in synthetic organic chemistry. Overall, its characteristics make it a versatile compound in both academic research and industrial applications.
Formula:C13H26BNO2Si
InChI:InChI=1/C13H26BNO2Si/c1-10(2)18(11(3)4,12(5)6)15-8-7-13(9-15)14(16)17/h7-12,16-17H,1-6H3
SMILES:CC(C)[Si](C(C)C)(C(C)C)n1ccc(c1)B(O)O
Synonyms:
  • {1-[tris(propan-2-yl)silyl]-1H-pyrrol-3-yl}boronic acid
  • {1-[tris(1-methylethyl)silyl]-1H-pyrrol-3-yl}boronic acid
  • 1-(TRIISOPROPYLSILYL)PYRROLE-3-BORONIC ACID
  • 1-Tris(isopropylsilyl)-1H-pyrrole-3-boronic acid
  • 1-(TRIISOPROPYLSILYL)-1H-PYRROLE-3-BORONIC ACID
  • RARECHEM AH PB 0020
  • AKOS BRN-0345
  • 1-(triisopropylsilyl)-1H-pyrrol-3-ylboronic acid
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