Identification | Back Directory | [Name]
1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE) | [CAS]
165535-45-5 | [Synonyms]
P2Et Phosphazene Phosphazene base P PHOSPHAZENE BASE P2-ET Phosphazene base P2-Et >=98.0% (NT) TETRAMETHYL(TRIS(DIMETHYLAMINO)PHOSPHOR& Phosphazene base P2-Et purum, >=98.0% (NT) 1-ethyl-2,2,4,4,4-pentakis(dimethylamino)-2λ5,4λ5-catenadi(phosphazene) Tetramethyl(tris(dimethylamino)phosphoranylidene)phosphorictriamid-Et-imin 1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE) N,N,N',N'-TETRAMETHYL-N''-[TRIS(DIMETHYLAMINO)PHOSPHORANYLIDENE]PHOSPHORIC TRIAMIDE ETHYLIMINE N',N',N'',N''-hexamethylphosphorimidic triamide-N,N,N',N',N'',N''-hexamethylphosphorimidic triamide Phosphorimidic triamide, N'''-[P,P-bis(dimethylamino)-N-ethylphosphinimyl]-N,N,N',N',N'',N''-hexamethyl- 2,n'3,n'3,n3,n3,n'5,n'5,n5,n5-Nonamethyl-2,4,6-triaza-3lambda5,5lambda5-diphosphaocta-3,5-diene-3,3,5,5-tetramine 2,n'3,n'3,n3,n3,n'5,n'5,n5,n5-Nonamethyl-2,4,6-triaza-3lambda5,5lambda5-diphosphaocta-3,5-diene-3,3,5,5-tetramine N-[dimethylamino-ethylimino-[[tris(dimethylamino)-$l^{5}-phosphanylidene]amino]-$l^{5}-phosphanyl]-N-methylmethanamine N-[dimethylamino-ethylimino-[[tris(dimethylamino)-λsup5sup-phosphanylidene]amino]-λsup5sup-phosphanyl]-N-methylmethanamine 1-Ethyl-2,2,4,4,4-pentakis(dimethylamino)-2λ5,4λ5-catenadi(phosphazene), Tetramethyl(tris(dimethylamino)phosphoranylidene)phosphorictriamid-Et-imin | [Molecular Formula]
C12H35N7P2 | [MDL Number]
MFCD00145113 | [MOL File]
165535-45-5.mol | [Molecular Weight]
339.4 |
Chemical Properties | Back Directory | [Boiling point ]
96 °C0.05 mm Hg(lit.) | [density ]
1.02 g/mL at 25 °C(lit.) | [refractive index ]
n20/D 1.492(lit.) | [Fp ]
113 °C | [form ]
liquid | [BRN ]
7485991 |
Hazard Information | Back Directory | [Uses]
P2Et phosphazene is a strong non-ionic base has the ability to catalyze a wide variety of organic transformations. This includes but is not limited to cross coupling reactions, deprotonation of sulphones and conversion of vinyl sufone to allyl sulfone |
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