Company Name: |
J & K SCIENTIFIC LTD.
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Tel: |
010-82848833 400-666-7788 |
Email: |
jkinfo@jkchemical.com |
Products Intro: |
Product Name:N-Methoxy-N-methyl-2-(triphenylphosphoranylidene)acetamide, 98% CAS:129986-67-0 Purity:98% Package:5GR, 25GR
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Company Name: |
Meryer (Shanghai) Chemical Technology Co., Ltd.
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Tel: |
021-61259108 18621169085 |
Email: |
market03@meryer.com |
Products Intro: |
Product Name:N-Methoxy-N-Methyl-2-(triphenylphosphoranylidene)acetaMide CAS:129986-67-0 Purity:98% Remarks:39009
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| N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE Basic information |
Product Name: | N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE | Synonyms: | N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE;N-METHOXY-N-METHYL-2-(TRIPHENYLPHOSPHORANYLIDENE)ACETAMIDE;[N-METHOXYMETHYLAMINOCARBONYLMETHYLENE]-TRIPHENYLPHOSPHORANE;N-Methoxy-N-methyl-2-(triphenylphosphoranylidene)acetamide, 98 %;(N-methoxymethylaminocarbonylmethylene)triphenylphosphoran;N-Methoxy-N-methyl(triphenylphosphoranylidene)acetamide 98%;N-methoxy-N-methyl-2-(triphenyl-l5-phosphanylidene)acetamide;Acetamide, N-methoxy-N-methyl-2-(triphenylphosphoranylidene)- | CAS: | 129986-67-0 | MF: | C22H22NO2P | MW: | 363.39 | EINECS: | | Product Categories: | | Mol File: | 129986-67-0.mol | ![N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE Structure](CAS/GIF/129986-67-0.gif) |
| N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE Chemical Properties |
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 Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36 | WGK Germany | 3 | F | 9 | HS Code | 29241900 |
| N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE Usage And Synthesis |
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
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| N-METHOXY-N-METHYL(TRIPHENYL-PHOSPHORANYLIDENE)ACETAMIDE Preparation Products And Raw materials |
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