Diisopropyl phosphite

CAS : 1809-20-7

Ref. 3D-FD22140

Informations sur le produit

• Nom: Diisopropyl phosphite
• Synonymes: Diisopropyl phosphonatePhosphonic acid diisopropyl esterPhosphorous acid diisopropyl ester, 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 ((C₃H₇O)₂(HO)P), Isopropyl phosphonate ((C₃H₇O)₂HPO), 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)

Description

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.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 166.16 g/mol
• Formule: C₆H₁₅O₃P
• Degré de pureté: Min. 98 Area-%
• Couleur/Forme: Clear Liquid
• InChI: InChI=1S/C6H15O3P/c1-5(2)8-10(7)9-6(3)4/h5-7H,1-4H3
• Code InChI: InChIKey=NFORZJQPTUSMRL-UHFFFAOYSA-N
• SMILES: CC(C)OP(O)OC(C)C