2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE
2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE Basic information
- Product Name:
- 2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE
- Synonyms:
-
- 2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE,2,8,9-TRIS(1-METHYLETHYL)
- 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
- 2,8,9-TRIISOPROPYL-2,5,8,9-TETRAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE
- 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 solution 1 M in toluene
- 4,6,11-tri(propan-2-yl)-1,4,6,11-tetraza-5-phosphabicyclo[3.3.3]undecane
- CAS:
- 175845-21-3
- MF:
- C15H33N4P
- MW:
- 300.42
- Product Categories:
-
- Chemical Synthesis
- Organic Bases
- Synthetic Reagents
- organic phosphine
- Mol File:
- 175845-21-3.mol
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2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE Chemical Properties
- Boiling point:
- 351.4±41.0 °C(Predicted)
- Density
- 0.922 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.4830(lit.)
- Flash point:
- 46 °F
- pka
- 9.37±0.20(Predicted)
- form
- liquid
- color
- yellow
- Specific Gravity
- 0.922
- Sensitive
- moisture sensitive
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Safety Information
- Hazard Codes
- F,Xn
- Risk Statements
- 11-38-48/20-63-65-67
- Safety Statements
- 36/37-62-24/25-16
- RIDADR
- UN 1294 3/PG 2
- WGK Germany
- 3
MSDS
- Language:English Provider:SigmaAldrich
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2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE Usage And Synthesis
Reaction
Exceedingly strong, non-ionic Brønsted and Lewis base useful in a variety of organic transformations.
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
2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANESupplier
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