DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE
  • CAS No.:24074-26-8
Other grades of this product :
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE Basic information
Product Name:DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE
Synonyms:DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE;Diisopropyl (carboethoxymethyl)phosphonate;Ethyl (diisopropyl phosphono)acetate;Acetic acid, 2-[bis(1-methylethoxy)phosphinyl]-, ethyl ester;ethyl 2-di(propan-2-yloxy)phosphorylacetate;Ethyl 2-(diisopropoxyphosphoryl)acetate
CAS:24074-26-8
MF:C10H21O5P
MW:252.24
EINECS:
Product Categories:C-C Bond Formation;Horner-Wadsworth-Emmons Reagents;Olefination
Mol File:24074-26-8.mol
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE Chemical Properties
Boiling point 142-143 °C11 mm Hg(lit.)
density 1.06 g/mL at 25 °C(lit.)
refractive index n20/D 1.427(lit.)
Fp >230 °F
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE Usage And Synthesis
UsesReactant for:
  • Preparation of spiroimine ring fragment of spirolides via stereoselective intermolecular Diels-Alder and aza-Wittig cyclization
  • Katsuki-Sharpless epoxidation reaction
  • Preparation of nine-membered diallylic sulfonamides as chiral building blocks
  • Alpha-phosphono lactams for subsequent Wadsworth-Emmons olefination, and Suzuki coupling reactions to yield diverse pyrrolidinone compounds
  • Synthesis of galactosylceramide analog that induces Th1-biased responses in human (NKT) cells
  • Stereoselective total synthesis of the ionophore antibiotic zincophorin (M144255)
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE Preparation Products And Raw materials

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