| Weight | 208.238 g/mol |
|---|---|
| Formula | C9H21O3P |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
TRIISOPROPYL PHOSPHITE (116-17-6)
phosphorous acid, triisopropyl ester · triisopropylphosphite
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- Low valent cobalt triisopropyl phosphite complexes. Characterization of a catalyst for the hydrogenation of .alpha.,.beta.-unsaturated ketones (Journal of the American Chemical Society, 1977)
- Mitsunobu reactions of nucleoside analogs using triisopropyl phosphiteDIAD (Tetrahedron Letters, 2006)
- Organocobalt B12 models and very long cobalt-carbon (tertiary) bonds. Synthesis and spectroscopic, kinetic, and structural properties of trans-bis(dimethylglyoximato)adamantyl(L)cobalt(III) with L = trimethyl phosphite and triisopropyl phosphite (Organometallics, 1985)
- Mechanism of photosubstitution of (.eta.5-C5H5)2Fe2(CO)4 by triphenylphosphine and triisopropyl phosphite. Direct observation of a binuclear intermediate, (.eta.5-C5H5)2Fe2(CO)4{P[OCH(CH3)2]3}, a molecule with a carbonyl bridge but no metal-metal bond (Journal of the American Chemical Society, 1979)
- Electrochemistry of coordination compounds: XXIII. Rhodium(0): Electrogeneration and characterization of tetrakis(triisopropyl-phosphite)rhodium (Journal of Organometallic Chemistry, 1986)
- Reduction of Carbonyl Compounds to Hydrocarbons with Triisopropyl Phosphite: An Inexpensive New Reducing Agent1 (Synlett, 1990)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phosphorous acid, triisopropyl ester
- triisopropylphosphite
-
SMILESCC(C)OP(OC(C)C)OC(C)C
-
InChIKeySJHCUXCOGGKFAI-UHFFFAOYSA-N
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TRIISOPROPYL PHOSPHITE
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