Organic phosphines
+ Tert-butyl phosphines
+ Cyclohexyl phosphines
+ Phenyl phosphines
+ Chiral Phosphines
+ H-P phosphines
+ Other organic phosphines
Metal phosphine complexes
OLED intermediates
+ Fluorenes
+ Carbazoles
+ Boric acids
+ Thiophenes
Norbornenes
Functional intermediates
Acid Anhydrides
+ Tert-butyl phosphines
+ Cyclohexyl phosphines
+ Phenyl phosphines
+ Chiral Phosphines
+ H-P phosphines
+ Other organic phosphines
Metal phosphine complexes
OLED intermediates
+ Fluorenes
+ Carbazoles
+ Boric acids
+ Thiophenes
Norbornenes
Functional intermediates
Acid Anhydrides
Research and Development
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Advantageous reaction; Conditions of experiment and production:
◆ Temperature ranges of synthesis reaction: -100 ℃ ~ 300 ℃, pressure: 10MPa.
◆Main reaction types: Diels-Alder reaction, catalytic hydrogenation reaction, reduction reaction, halogenation reaction, Suzuki reaction, Buchwald-Hartwig reaction, Ullmann reaction.