| Identification | Back Directory | [Name]
N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE | [CAS]
129986-67-0 | [Synonyms]
N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE
N-METHOXY-N-METHYL-2-(TRIPHENYLPHOSPHORANYLIDENE)ACETAMIDE
(N-methoxymethylaminocarbonylmethylene)triphenylphosphoran
N-Methoxy-N-methyl(triphenylphosphoranylidene)acetamide 98%
N-methoxy-N-methyl-2-(triphenyl-l5-phosphanylidene)acetamide
[N-METHOXYMETHYLAMINOCARBONYLMETHYLENE]-TRIPHENYLPHOSPHORANE
N-Methoxy-N-methyl-2-(triphenylphosphoranylidene)acetamide, 98 % | [Molecular Formula]
C22H22NO2P | [MDL Number]
MFCD00144930 | [MOL File]
129986-67-0.mol | [Molecular Weight]
363.39 |
| Chemical Properties | Back Directory | [Appearance]
White to off-white powder | [Melting point ]
183 °C | [Boiling point ]
495.6±28.0 °C(Predicted) | [density ]
1.18±0.1 g/cm3(Predicted) | [storage temp. ]
-20°C Freezer, Under inert atmosphere | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
Off White to Pale Yellow | [BRN ]
4198472 |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white powder | [Uses]
Reactant for:
- Synthesis of electron-deficient alkenes via stereoselective olefination of N-sulfonyl imines
- Phosphine-catalyzed asymmetric addition reactions
- Cysteine-catalyzed enantioselective intramolecular Rauhut-Currier reaction
- Wittig olefination
- Synthesis of aigialomycin D, a Protein Kinase inhibitor and a potential anticancer agent
| [reaction suitability]
reaction type: C-C Bond Formation |
|
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