CAS 1809-20-7
:Fosfito di diisopropile
- 2-Propan-2-yloxyphosphonoyloxypropane
- Bis(1-Methylethoxy)(Oxo)Phosphonium
- Bis(2-propyl) phosphite
- Di-i-propylphosphite
- Diipropylphosphitemincolorlessliq
- Diisopropoxyphosphine oxide
- Diisopropyl Phosphonate
- Diisopropyl hydrogen phosphite
- Diisopropyl phosphate
- Dipropan-2-Yl Hydrogen Phosphite
- Dipropan-2-Yl Phosphonate
- Isopropyl phosphite ((C<sub>3</sub>H<sub>7</sub>O)<sub>2</sub>(HO)P)
- Isopropyl phosphonate ((C<sub>3</sub>H<sub>7</sub>O)<sub>2</sub>HPO)
- NSC 82344
- O,O-Diisopropyl phosphonate
- Phosphonic Acid Diisopropyl Ester
- Phosphonic acid, bis(1-methylethyl) ester
- T 451
- T 451 (antiwear additive)
- Isopropyl phosphonate ((C3H7O)2HPO)
- Vedi altri sinonimi
Diisopropyl Phosphite
CAS:Formula:C6H15O3PPurezza:>98.0%(GC)Colore e forma:Colorless to Almost colorless clear liquidPeso molecolare:166.16Diisopropyl phosphite, 98%
CAS:Diisopropyl phosphite is used as antiwear lubricant additive together with triphenyl thiophosphate on T8 steel/Al2O3 ceramics. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy branFormula:C6H14O3PPurezza:98%Colore e forma:Liquid, Clear colorlessPeso molecolare:165.15Di-i-propylphosphite, min. 98%
CAS:Di-i-propylphosphite, min. 98%
Formula:(C3H7O)2P(O)HPurezza:min. 98%Colore e forma:colorless liq.Peso molecolare:166.16Phosphonic acid, bis(1-methylethyl) ester
CAS:Formula:C6H15O3PPurezza:98%Colore e forma:LiquidPeso molecolare:166.1553Diisopropyl hydrogen phosphite
CAS:Formula:C6H15O3PPurezza:95.0%Colore e forma:Liquid, ClearPeso molecolare:166.157Diisopropyl Phosphite
CAS:Prodotto controllatoApplications Used as antiwear lubricant additive together with triphenyl thiophosphate on T8 steel/Al2O3 ceramics.
References Jiang, S., et al.: Wear, 268, 777 (2010),Formula:C6H15O3PColore e forma:NeatPeso molecolare:166.16Diisopropyl phosphite
CAS:Diisopropyl phosphite is a pyrimidine compound that is used in organic synthesis. It is an intermediate in the asymmetric synthesis of various pyridines. Diisopropyl phosphite reacts with hydrochloric acid to produce hydroxybenzoic acid and hydrogen gas. The first step in the reaction mechanism involves a palladium-catalyzed coupling reaction between diisopropyl phosphite and methyl iodide, which leads to the formation of a tetrahydrofuran ring system. Such reactions are generally carried out at low temperatures to minimize decomposition of diisopropyl phosphite. Diisopropyl phosphite has been shown to be chemically stable, but has low bioavailability due to its high reactivity with biological molecules such as proteins and lipids.
Formula:C6H15O3PPurezza:Min. 98 Area-%Colore e forma:Clear LiquidPeso molecolare:166.16 g/mol







