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CAS 740815-37-6

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2-[Bis(1,1-dimethylethyl)phosphino]-1-phenyl-1H-indole

Description:
2-[Bis(1,1-dimethylethyl)phosphino]-1-phenyl-1H-indole is a chemical compound characterized by its unique structure, which includes a phosphine group and an indole moiety. The presence of the bis(1,1-dimethylethyl) substituents on the phosphorus atom enhances its steric bulk, making it a bulky ligand often used in coordination chemistry and catalysis. This compound is typically utilized in the synthesis of various organometallic complexes, particularly in transition metal catalysis, due to its ability to stabilize metal centers and influence reactivity. The indole ring contributes to its aromatic properties, which can affect the electronic characteristics of the compound. Additionally, the compound may exhibit interesting biological activities, although specific biological data may vary. Its synthesis and handling require standard laboratory safety protocols, as with many organophosphorus compounds, due to potential toxicity and reactivity. Overall, this compound is significant in both academic research and industrial applications, particularly in the fields of catalysis and materials science.
Formula:C22H28NP
InChI:InChI=1S/C22H28NP/c1-21(2,3)24(22(4,5)6)20-16-17-12-10-11-15-19(17)23(20)18-13-8-7-9-14-18/h7-16H,1-6H3
InChI key:InChIKey=HDZRDZCQFYUOHE-UHFFFAOYSA-N
SMILES:P(C(C)(C)C)(C(C)(C)C)C=1N(C=2C(C1)=CC=CC2)C3=CC=CC=C3
Synonyms:
  • 2-(Di-Tert-Butylphosphino)-1-Phenylindole
  • 2-[Bis(1,1-dimethylethyl)phosphino]-1-phenyl-1H-indole
  • N-Phenyl-2-(di-tert-butylphosphino)indole
  • N-Phenylindol-2-yl-di-tert-butylphosphine
  • 1H-Indole, 2-[bis(1,1-dimethylethyl)phosphino]-1-phenyl-
  • 2-(Di-tert-butylphosphino)-1-phenylindole 96%
  • 2-(di-tert-butylphosphino)-1-phenyl-1H-indole
  • 98% [cataCXiuM PIntB]
  • N-Phenyl-2-(di-t-butylphosphino)indol,98%
  • cataCXium(R) PIntB
  • See more synonyms
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