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Details
Excellent chemical plant bulk supply Diisopropyl phosphite 1809-20-7
- Molecular Formula: C6H15O3P
- Molecular Weight: 166.157
- Appearance/Colour: clear, colorless clear liquid.
- Vapor Pressure: 0.586mmHg at 25°C
- Refractive Index: 1.4065-1.4085
- Boiling Point: 195.513 °C at 760 mmHg
- Flash Point: 90.254 °C
- PSA： 52.28000
- Density: 0.997 g/cm3
- LogP: 2.05560
Diisopropyl phosphite(Cas 1809-20-7) Usage
|
Synthesis Reference(s) |
Tetrahedron Letters, 29, p. 3327, 1988 DOI: 10.1016/0040-4039(88)85153-0 |
InChI:InChI=1/C6H15O3P/c1-5(2)8-10(7)9-6(3)4/h5-6,10H,1-4H3
1809-20-7 Relevant articles
Way to Enforce Selectivity via Steric Hindrance: Improvement of Am(III)/Eu(III) Solvent Extraction by Loaded Diphosphonic Acid Esters
Matveev, Petr I.,Huang, Pin-Wen,Kirsanova, Anna A.,Ananyev, Ivan V.,Sumyanova, Tsagana B.,Kharcheva, Anastasia V.,Khvorostinin, Evgenii Yu.,Petrov, Vladimir G.,Shi, Wei-Qun,Kalmykov, Stepan N.,Borisova, Nataliya E.
, p. 14563 - 14581 (2021/10/12)
Hybrid donor extractants are a promising...
Copper-Catalyzed C?P Cross-Coupling of (Cyclo)alkenyl/Aryl Bromides and Secondary Phosphine Oxides with in situ Halogen Exchange
Stankevi?, Marek,Wo?nicki, Pawe?
supporting information, p. 3484 - 3491 (2021/07/22)
An efficient protocol for concurrent tan...
Reaction of sodium N-benzylideneglycinate with dialkyl chlorophosphites in the presence of water
Dimukhametov, Mudaris N.,Mironov, Vladimir F.,Islamov, Daut R.,Litvinov, Igor A.,Gnezdilov, Oleg I.,Danilova, Yuliya V.
, p. 107 - 109 (2021/02/16)
The outcome of reaction of sodium N-benz...
METHOD FOR PRODUCING ORGANOPHOSPHORUS COMPOUND
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Paragraph 0085; 0090; 0091; 0094; 0095, (2020/05/02)
PROBLEM TO BE SOLVED: To provide a metho...
1809-20-7 Process route
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67-63-0,8013-70-5
isopropyl alcohol
-
-
1809-20-7
diisopropyl hydrogenphosphonate
| Conditions | Yield |
|---|---|
|
With
pyridine; phosphorus trichloride;
In
diethyl ether;
at 0 - 20 ℃;
|
99%
|
|
With
phosphorus trichloride;
Cooling;
|
92.1%
|
|
With
phosphorus trichloride;
at 5 ℃;
|
90%
|
|
With
phosphorus trichloride;
|
90%
|
|
With
phosphorus trichloride;
In
pyridine; diethyl ether;
for 2h;
cooling;
|
89%
|
|
With
phosphorus trichloride;
In
dichloromethane;
for 0.166667h;
|
84%
|
|
With
phosphorus trichloride;
In
dichloromethane;
at 0 - 10 ℃;
for 17h;
|
81%
|
|
With
phosphorus trichloride;
|
|
|
With
diethyl ether; phosphorus trichloride;
|
|
|
With
phosphorus trichloride;
|
|
|
With
tetrachloromethane; phosphorus trichloride;
|
|
|
With
phosphorus trichloride;
In
tetrachloromethane;
|
|
|
With
phosphorus trichloride;
|
|
|
With
phosphorus trichloride;
at 0 - 50 ℃;
for 2h;
|
|
|
With
phosphorus trichloride;
|
|
|
With
diethyl ether; water;
anschliessendes Behandeln mit Phosphor(III)-chlorid;
|
|
|
With
water; chlorobenzene;
anschliessendes Behandeln mit Phosphor(III)-chlorid;
|
-
-
14540-27-3
diisopropyl ethyl phosphite
-
-
67-64-1
acetone
-
-
1809-20-7
diisopropyl hydrogenphosphonate
| Conditions | Yield |
|---|---|
|
|
1809-20-7 Upstream products
-
67-63-0
isopropyl alcohol
-
14540-27-3
diisopropyl ethyl phosphite
-
67-64-1
acetone
-
107-10-8
propylamine
1809-20-7 Downstream products
-
55-91-4
diisopropyl phosphofluoridate
-
15175-95-8
diisopropyl N,N-diethylcarbamoylphosphonate
-
60324-11-0
diisopropyl (1-hydroxy-1-cyclohexyl)phosphonate
-
107620-03-1
(α-hydroxy-3-nitro-benzyl)-phosphonic acid diisopropyl ester
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