| Identification | Back Directory | [Name]
2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE | [CAS]
175845-21-3 | [Synonyms]
2,8,9-TRIISOPROPYL-2,5,8,9-TETRAAZA-1-P&
2,8,9-TRIISOPROPYL-2,5,8,9-TETRAZA-1-PH&
2,8,9-TRIISOPROPYL-2,5,8,9-TETRAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE
2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE
2,8,9-TRIISOPROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE
4,6,11-tri(propan-2-yl)-1,4,6,11-tetraza-5-phosphabicyclo[3.3.3]undecane
2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE,2,8,9-TRIS(1-METHYLETHYL)
2,8,9-Tris(1-methylethyl)-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane
2,8,9-triisopropyl-2,5,8,9-tetraza-1-phosphabicyclo[3.3.3]undecane solution
2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane solution
2,8,9-Triisopropyl-2,5,8,9-tetraza-1-phosphabicyclo[3.3.3]undecane solution 1 M in toluene | [Molecular Formula]
C15H33N4P | [MDL Number]
MFCD03701530 | [MOL File]
175845-21-3.mol | [Molecular Weight]
300.42 |
| Chemical Properties | Back Directory | [Boiling point ]
351.4±41.0 °C(Predicted) | [density ]
0.922 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.4830(lit.)
| [Fp ]
46 °F
| [form ]
liquid | [pka]
9.37±0.20(Predicted) | [color ]
yellow | [Specific Gravity]
0.922 | [Sensitive ]
moisture sensitive | [InChI]
1S/C15H33N4P/c1-13(2)17-10-7-16-8-11-18(14(3)4)20(17)19(12-9-16)15(5)6/h13-15H,7-12H2,1-6H3 | [InChIKey]
DFRWCJYSXGNOFD-UHFFFAOYSA-N | [SMILES]
CC(C)N1CCN2CCN(C(C)C)P1N(CC2)C(C)C |
| Hazard Information | Back Directory | [Uses]
Base used in an attempt to produce higherly reactive no-carrier-added fluoride for labeling of radiopharmaceuticals and used in the synthesis of monomeric alumatranes
Deprotonation agent used to study the nucleophilic reactivities of benzenesulfonyl-substituted carbanions
Catalyst involved in:
- Synthesis of polymer-supported proazaphosphatranes for catalysis of amidation and transesterification reactions
- Wadsworth-Emmons reactions
- Mukaiyama aldol reactions
- Synthesis of aryl alcohols via addition reactions
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