ChemicalBook >?? ???? >?? ??>?? ??>? ?? ???>2,8,9-Tri-i-butyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane
2,8,9-Tri-i-butyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane
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2,8,9-Tri-i-butyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane ??
- ?? ?
- 397.4±41.0 °C(Predicted)
- ??
- 0.964 g/mL at 25 °C(lit.)
- ???
- n
20/D 1.5020(lit.)
- ???
- 155 °F
- ?? ??
- under inert gas (nitrogen or Argon) at 2-8°C
- ?? ?? (pKa)
- 8.90±0.20(Predicted)
- ??? ??
- ??
- ??
- ??~???? ???
- ??
- air sensitive, moisture sensitive
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- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
??? ?? | F,Xn | ||
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?? ???? ?? | 36/37/38-67-66-22-19-11 | ||
????? | 26-36/37/39-16 | ||
????(UN No.) | UN1155 - class 3 - PG 1 - Diethyl ether | ||
WGK ?? | 3 | ||
HS ?? | 29310099 |
????(GHS): | ||||||||||||||||||||||||||||||||||||
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?? ?: | Danger | |||||||||||||||||||||||||||||||||||
??·?? ??: |
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2,8,9-Tri-i-butyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane C??? ??, ??, ??
??? ??
Clear colorless to yellow liquid??
Triisobutylazaphosphatrane is reported to be used as a catalyst for the preparation of biaryl and alkenylarenes via Stille cross-coupling reaction. It also acts a catalyst for the synthesis of α-aryl-substituted nitriles.2,8,9-Tri-i-butyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane ?? ?? ? ???
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2,8,9-Tri-i-butyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane ?? ??
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