124931-12-0

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124931-12-0 Structure

Identification	Back Directory
[Name] DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE
[CAS] 124931-12-0
[Synonyms] Diethyl (2-(methoxy(methyl) N-Methoxy-N-methyl-diethylphosphoacetamide DIETHYL N-METHOXY-N-METHYLPHOSPHONOACETAMIDE N-Methoxy-N-methyl-2-(diethyl phosphono)acetamide 2-diethoxyphosphoryl-N-methoxy-N-methyl-acetamide N-METHOXY-N-METHYL-PHOSPHONOACETAMIDE DIETHYL ESTER Diethylphosphonoacetic acid N-methyl-N-methoxyamide diethyl (N-ethoxy-N-methylcarbamoylmethyl)phosphonate DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE Diethyl (2-(Methoxy(Methyl)aMino)-2-oxoethyl)phosphonate Diethyl(N-Methoxy-N-methylcarbamoylmethyl)phosphonate> Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate ,97% Diethyl(N-methoxy-N-methylcarbamoylmethyl)phosphonate, min. 97 % (N-Methoxy-N-methylcarbamoylmethyl)phosphonic Acid Diethyl Ester Diethyl (N-Methoxy-N-methylcarbamoylmethyl)phosphonate Phosphonic acid,P-[2-(methoxymethylamino)-2-oxoethyl]-, diethyl ester Diethyl N-methoxy-N-methylphosphonoacetamide, N-Methoxy-N-methyl-phosphonoacetamide diethyl ester
[Molecular Formula] C8H18NO5P
[MDL Number] MFCD00134233
[MOL File] 124931-12-0.mol
[Molecular Weight] 239.21

Chemical Properties	Back Directory
[Boiling point ] 90 °C17 mm Hg(lit.)
[density ] 1.163 g/mL at 25 °C(lit.)
[refractive index ] n20/D 1.455(lit.)
[Fp ] >230 °F
[form ] clear liquid
[color ] Colorless to Almost colorless
[BRN ] 1875865
[CAS DataBase Reference] 124931-12-0

Raw materials And Preparation Products	Back Directory
[Raw materials] Dichloromethane-->Triethylamine-->Triethyl phosphite-->Bromoacetyl bromide-->N,O-Dimethylhydroxylamine hydrochloride
[Preparation Products] (2E)-N-methoxy-3-(2-methoxyphenyl)-N-methylprop-2-enamide-->3-(4-chlorophenyl)-N-methoxy-N-methylacrylamide-->(2E)-N-methoxy-3-(4-methoxyphenyl)-N-methylprop-2-enamide

Hazard Information	Back Directory
[Uses] Reactant for: Preparation of ring-expanded bryostatin analogs as antitumor agents Asymmertic synthesis of pinnatoxins A and G via diastereoselective Ireland-Claisen rearrangement, ring closing metathesis, and cyclization Rh2(II)-catalyzed nitro-group migration reactions Stereoselective synthesis of cyclohexanones via phase transfer catalyzed double addition reactions Stereoselective synthesis of (+)-polyrhacitide A via aldol reaction, Horner-Wardsworth-Emmons reaction, Evans acetal intramolecular oxa-Michael reaction and diastereoselective syn reduction reaction as the key steps Preparation of substituted furans via olefin cross-metathesis
[reaction suitability] reaction type: C-C Bond Formation

Spectrum Detail	Back Directory
[Spectrum Detail] DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE(124931-12-0)¹HNMR DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE(124931-12-0)FT-IR DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE(124931-12-0)Raman DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE(124931-12-0)IR

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