4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine
4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine Basic information
- Product Name:
- 4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine
- Synonyms:
-
- 4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine
- PyriMidine, 4-(3,5-dibroMophenyl)-2,6-diphenyl-
- -2,6-diphenylpyrimidine
- 4-(3,5-Dibromophenyl)
- 4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine>
- 4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine ISO 9001:2015 REACH
- CAS:
- 607740-08-9
- MF:
- C22H14Br2N2
- MW:
- 466.17
- Product Categories:
-
- pyrimidine
- Mol File:
- 607740-08-9.mol
4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine Chemical Properties
- Melting point:
- 197.0 to 201.0 °C
- Boiling point:
- 476.7±45.0 °C(Predicted)
- Density
- 1.532
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- pka
- -0.65±0.41(Predicted)
- color
- White to Almost white
- CAS DataBase Reference
- 607740-08-9
4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine Usage And Synthesis
Uses
4-(3,5-dibromophenyl)-2,6-diphenylpyrimidine is an organic intermediate that can be prepared in two steps by reacting 3,5-dibromobenzaldehyde, acetophenone and benzamide hydrochloride.
Synthesis
56990-02-4
1670-14-0
98-86-2
607740-08-9
3,5-dibromobenzaldehyde (1.0 g, 40 mmol), acetophenone (4.81 g, 40 mmol) were used as raw materials, which were dissolved in ethanol (80 mL), followed by addition of sodium hydroxide (0.16 g, 4 mmol). The reaction mixture was stirred at room temperature for 8 hours. Upon completion of the reaction, benzylcarbamidine hydrochloride (4.70 g, 30 mmol), sodium hydroxide (1.60 g, 40 mmol) and ethanol (40 mL) were added to the system and the reaction mixture was heated to reflux and the reaction was continued for 8 hours. At the end of the reaction, the resulting white solid was collected by filtration and washed with ethanol until the filtrate was colorless. The solid product was further washed with water and ethanol and finally dried under vacuum to give intermediate N (5.20 g, yield: 56%).
References
[1] Patent: EP2662368, 2013, A1. Location in patent: Paragraph 0183; 0184
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