1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE)
1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE) Basic information
- Product Name:
- 1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE)
- Synonyms:
-
- 1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE)
- TETRAMETHYL(TRIS(DIMETHYLAMINO)PHOSPHOR&
- N,N,N',N'-TETRAMETHYL-N''-[TRIS(DIMETHYLAMINO)PHOSPHORANYLIDENE]PHOSPHORIC TRIAMIDE ETHYLIMINE
- PHOSPHAZENE BASE P2-ET
- 1-ethyl-2,2,4,4,4-pentakis(dimethylamino)-2λ5,4λ5-catenadi(phosphazene)
- 1-Ethyl-2,2,4,4,4-pentakis(dimethylamino)-2λ5,4λ5-catenadi(phosphazene), Tetramethyl(tris(dimethylamino)phosphoranylidene)phosphorictriamid-Et-imin
- Phosphazene base P2-Et purum, >=98.0% (NT)
- Tetramethyl(tris(dimethylamino)phosphoranylidene)phosphorictriamid-Et-imin
- CAS:
- 165535-45-5
- MF:
- C12H35N7P2
- MW:
- 339.4
- Mol File:
- 165535-45-5.mol
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1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE) Chemical Properties
- Boiling point:
- 96 °C0.05 mm Hg(lit.)
- Density
- 1.02 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.492(lit.)
- Flash point:
- 113 °C
- storage temp.
- 2-8°C, protect from light, stored under nitrogen
- form
- liquid
- Appearance
- Colorless to light yellow Liquid
- BRN
- 7485991
- InChI
- 1S/C12H35N7P2/c1-12-13-20(15(2)3,16(4)5)14-21(17(6)7,18(8)9)19(10)11/h12H2,1-11H3
- InChIKey
- CFUKEHPEQCSIOM-UHFFFAOYSA-N
- SMILES
- CCN=P(N=P(N(C)C)(N(C)C)N(C)C)(N(C)C)N(C)C
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Safety Information
- Hazard Codes
- C
- Risk Statements
- 34
- Safety Statements
- 26-36/37/39-45-27
- RIDADR
- UN 3267 8/PG 2
- WGK Germany
- 3
- F
- 3-10-21-34
- Storage Class
- 8A - Combustible corrosive hazardous materials
- Hazard Classifications
- Skin Corr. 1B
MSDS
- Language:English Provider:SigmaAldrich
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1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE) Usage And Synthesis
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
1-ETHYL-2,2,4,4,4-PENTAKIS(DIMETHYLAMINO)-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENE)Supplier
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