2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE

CAS No.：175845-21-3

Other grades of this product :

2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE Basic information

Reaction

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
EINECS:
Product Categories:	Chemical Synthesis;Organic Bases;Synthetic Reagents;organic phosphine
Mol File:	175845-21-3.mol

2,8,9-TRI-I-PROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE Chemical Properties

density	0.922 g/mL at 25 °C(lit.)
refractive index	n20/D 1.4830(lit.)
Fp	46 °F
form	liquid
color	yellow
Specific Gravity	0.922
Sensitive	moisture sensitive

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 Information

Provider	Language
SigmaAldrich	English

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 alumatranesDeprotonation agent used to study the nucleophilic reactivities of benzenesulfonyl-substituted carbanionsCatalyst 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]UNDECANE Preparation Products And Raw materials

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