86030-43-5

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86030-43-5 Structure

Identification	Back Directory
[Name] CHLORO(DIISOPROPYLAMINO)METHOXYPHOSPHINE
[CAS] 86030-43-5
[Synonyms] CHLORO(DIISOPROPYLAMINO)METHOXYPHOSPHINE Methyl DiisopropylphosphoraMidochloridite METHYL N,N-DIISOPROPYLCHLOROPHOSPHORAMIDITE N,N-DIISOPROPYLMETHYLPHOSPHONAMIDIC CHLORIDE (N,N-DiisopropylaMino)Methoxychlorophosphine METHYL N,N-DIISOPROPYLPHOSPHORAMIDOCHLORIDITE 1-chloro-N,N-diisopropyl-1-methoxyphosphanamine N,N-Diisopropylmethylphosphonamidic chloride 95% N,N-Diisopropylamidochloridophosphorous acid methyl ester N,N-Diisopropylmethylphosphoramidic Chloride, 80% DISCONTINUED N,N-Bis(1-Methylethyl)phosphoraMidochloridous Acid Methyl Ester Phosphoramidochloridous acid, N,N-bis(1-methylethyl)-, methyl ester Chloro(diisopropylamino)methoxyphosphine, Methyl N,N-diisopropylchlorophosphoramidite, Methyl N,N-diisopropylphosphoramidochloridite
[Molecular Formula] C7H17ClNOP
[MDL Number] MFCD00009859
[MOL File] 86030-43-5.mol
[Molecular Weight] 197.64

Hazard Information	Back Directory
[Chemical Properties] Colourless Liquid
[Uses] N,N-Diisopropylmethylphosphoramidic Chloride is used in the synthesis of phosphorothioate analogs of platelet-activating factor.
[reaction suitability] reaction type: Buchwald-Hartwig Cross Coupling Reaction reaction type: Heck Reaction reaction type: Hiyama Coupling reaction type: Negishi Coupling reaction type: Sonogashira Coupling reaction type: Stille Coupling reaction type: Suzuki-Miyaura Coupling

Spectrum Detail	Back Directory
[Spectrum Detail] CHLORO(DIISOPROPYLAMINO)METHOXYPHOSPHINE(86030-43-5)MS CHLORO(DIISOPROPYLAMINO)METHOXYPHOSPHINE(86030-43-5)¹HNMR CHLORO(DIISOPROPYLAMINO)METHOXYPHOSPHINE(86030-43-5)¹³CNMR CHLORO(DIISOPROPYLAMINO)METHOXYPHOSPHINE(86030-43-5)IR1 CHLORO(DIISOPROPYLAMINO)METHOXYPHOSPHINE(86030-43-5)Raman

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