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diphenyl phenylphosphonite
diphenyl phenylphosphonate
Conditions | Yield |
---|---|
With dihydrogen peroxide In 1,4-dioxane; water at 8 - 12℃; for 1h; | 98.7% |
With tetrachloromethane; benzaldehyde |
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); Phenyl triflate In neat (no solvent) at 160℃; for 16h; Catalytic behavior; Reagent/catalyst; Temperature; Inert atmosphere; | 94% |
Multi-step reaction with 2 steps 1: tris-(dibenzylideneacetone)dipalladium(0) / diethyl ether / 50 °C / Inert atmosphere; Schlenk technique 2: tris-(dibenzylideneacetone)dipalladium(0) / N,N-dimethyl-formamide / 8 h / 160 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
With nickel dichloride; triethyl phosphite at 160℃; for 4h; Arbuzov reaction; | 93% |
With sodium dodecyl-sulfate; triethylamine In water at 100℃; for 2h; | 91% |
With triethylamine In neat (no solvent) at 100℃; for 5h; Green chemistry; | 79% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 35℃; for 16h; Inert atmosphere; Schlenk technique; Irradiation; | 89% |
Conditions | Yield |
---|---|
With 2,2':6,2''-terpyridine; cobalt(II) bromide; zinc In acetonitrile at 20℃; for 24h; | 84% |
Conditions | Yield |
---|---|
With sodium dodecyl-sulfate; triethylamine In water at 100℃; for 3h; | 81% |
With triethylamine In neat (no solvent) at 100℃; for 7h; Green chemistry; | 71% |
With copper(l) iodide; sodium hydride 1.) HMPT, 70-80 deg C; 2.) 150-160 deg C, 1 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With tert.-butylnitrite; salicylic acid In acetonitrile at 20℃; for 2h; Schlenk technique; Inert atmosphere; | 81% |
Stage #1: aniline With tert.-butylnitrite; toluene-4-sulfonic acid In acetonitrile at 0℃; for 0.25h; Sandmeyer Reaction; Stage #2: triphenyl phosphite In acetonitrile at 0.25℃; for 8h; Sandmeyer Reaction; | 79% |
With tert.-butylnitrite In dimethyl sulfoxide at 70℃; for 0.666667h; Sealed tube; |
P,P-dichlorophenylphosphine oxide
lithium phenolate
diphenyl phenylphosphonate
Conditions | Yield |
---|---|
In tetrahydrofuran at 0℃; Inert atmosphere; Reflux; | 80.2% |
In diethyl ether at -60℃; | 24% |
triphenyl phosphite
1-(methylsulfonyl)-2-(phenyl)diazene
diphenyl phenylphosphonate
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 24h; Inert atmosphere; Irradiation; | 77% |
diphenyl phenylphosphonate
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0) In N,N-dimethyl-formamide at 160℃; for 8h; Time; Inert atmosphere; | 53% |
Empirical Formula of Triphenyl phosphonate (CAS NO.3049-24-9): C18H15O3P
Molecular Weight: 310.2837 g/mol
EINECS: 221-261-9
Index of Refraction: 1.612
Density: 1.24 g/cm3
Flash Point: 224.4 °C
Enthalpy of Vaporization: 65.35 kJ/mol
Boiling Point: 425.2 °C at 760 mmHg
Vapour Pressure: 4.82E-07 mmHg at 25 °C
Structure of Triphenyl phosphonate (CAS NO.3049-24-9):
IUPAC Name: Diphenoxyphosphorylbenzene
Canonical SMILES: C1=CC=C(C=C1)OP(=O)(C2=CC=CC=C2)OC3=CC=CC=C3
InChI: InChI=1S/C18H15O3P/c19-22(18-14-8-3-9-15-18,20-16-10-4-1-5-11-16)21-17-12-6-2-7-13-17/h1-15H
InChIKey: CDOMXXVCZQOOMT-UHFFFAOYSA-N
1. | ipr-mus LD :>1250 mg/kg | CBCCT* “Summary Tables of Biological Tests“ National Research Council Chemical-Biological Coordination Center. 2 (1950),55. |
Moderately toxic by intraperitoneal route. When heated to decomposition Triphenyl phosphonate (CAS NO.3049-24-9) emits toxic vapors of POx.
Triphenyl phosphonate , its cas register number is 3049-24-9. It also can be called Diphenyl phenylphosphonate
; Diphenyl phenylphosphonate ; and Phosphonic acid, phenyl-, diphenyl ester .