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24074-26-8

24074-26-8 Structure

24074-26-8 Structure
IdentificationBack Directory
[Name]

DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE
[CAS]

24074-26-8
[Synonyms]

Ethyl (diisopropyl phosphono)acetate
Ethyl 2-(diisopropoxyphosphoryl)acetate
Diisopropyl (carboethoxymethyl)phosphonate
ethyl 2-di(propan-2-yloxy)phosphorylacetate
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE
Acetic acid, 2-[bis(1-methylethoxy)phosphinyl]-, ethyl ester
[Molecular Formula]

C10H21O5P
[MDL Number]

MFCD00075267
[MOL File]

24074-26-8.mol
[Molecular Weight]

252.24
Chemical PropertiesBack Directory
[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 DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37/39
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Reactant 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)
Spectrum DetailBack Directory
[Spectrum Detail]

DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE(24074-26-8)1HNMR
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE(24074-26-8)IR
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE(24074-26-8)Raman
DIISOPROPYL (ETHOXYCARBONYLMETHYL)PHOSPHONATE(24074-26-8)FT-IR
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