
Antioxidant BHT 264
CAS:128-37-0
Purity:99%
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Product Details
Chemical Properties |
Light yellow powder |
Purification Methods |
It has been recrystallised from AcOH, dioxane, AcOEt and Me2CO and dried it in a vacuum over P2O5. [Katelaar & Gersmann J Am Chem Soc 72 5777 1950, Moffatt & Khorana J Am Chem Soc 79 3741 1957.] |
InChI:InChI=1/C18H12N3O10P/c22-19(23)13-1-7-16(8-2-13)29-32(28,30-17-9-3-14(4-10-17)20(24)25)31-18-11-5-15(6-12-18)21(26)27/h1-12H
Phosphates and phosphonates compounds of...
We report the targeted decomposition of ...
The present invention refers to novel fl...
The invention discloses a process for pr...
4-nitro-phenol
tris(p-nitrophenyl)phosphate
4-chlorobenzonitrile
Conditions | Yield |
---|---|
With
phosphorus pentachloride;
|
4-nitro-phenol
tris(p-nitrophenyl)phosphate
Conditions | Yield |
---|---|
4-nitro-phenol;
With
sodium;
In
methanol; toluene;
at 30 - 45 ℃;
With
trichlorophosphate;
In
toluene;
for 0.0833333h;
Thermodynamic data;
Kinetics;
|
95% |
With
triethylamine; trichlorophosphate;
In
acetonitrile;
at 20 ℃;
for 1.16667h;
Cooling with ice;
|
77.6% |
With
triethylamine; trichlorophosphate;
In
acetonitrile;
at 20 ℃;
for 1.166h;
Inert atmosphere;
Cooling with ice;
|
|
With
pyridine; trichlorophosphate;
In
toluene;
at 110 ℃;
for 4h;
|
|
4-nitro-phenol;
With
sodium methylate;
In
methanol; toluene;
Heating;
With
trichlorophosphate;
In
toluene;
at 45 ℃;
Temperature;
Time;
Kinetics;
|
|
With
trichlorophosphate;
|
|
4-nitro-phenol;
With
triethylamine;
In
acetonitrile;
Inert atmosphere;
With
trichlorophosphate;
In
acetonitrile;
at 0 - 20 ℃;
for 1.16667h;
Inert atmosphere;
|
4-nitro-phenol
phosphoric acid triphenyl ester
4-(4-nitrophenoxy)butanoic acid
potassium 4-nitrophenolate
triethyl phosphate
bis(4-nitrophenyl) ethyl phosphate
1-nitro-4-octyloxybenzene
benzyl 4-nitrophenyl ether