N-méthoxy - N-méthyl(triphénylphosphoranylidène)acétamide, 98 %

Code: 376876-5G D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Reactant for: Synthesis of electron-deficient alkenes via stereoselective olefination of N-sulfonyl imines Phosphine-catalyzed asymmetric addition reactions Cyste...


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Votre prix
$141.35 5G
DEMANDER

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

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

Packaging

5, 25 g in glass bottle

assay98%
InChI keyDGBLSOOPDBHHRX-UHFFFAOYSA-N
InChI1S/C22H22NO2P/c1-23(25-2)22(24)18-26(19-12-6-3-7-13-19,20-14-8-4-9-15-20)21-16-10-5-11-17-21/h3-18H,1-2H3
mp173-175 °C (lit.)
reaction suitabilityreaction type: C-C Bond Formation
SMILES stringCON(C)C(=O)C=P(c1ccccc1)(c2ccccc2)c3ccccc3
Cas Number129986-67-0
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :



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