ChemicalBook >?? ???? >4-???-2,1,3-???????
4-???-2,1,3-???????
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4-???-2,1,3-??????? ??
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- 80 °C
- ?? ?
- 272.2±13.0 °C(Predicted)
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- 1.859±0.06 g/cm3(Predicted)
- ?? ??
- 2-8°C
- ?? ?? (pKa)
- -1.02±0.45(Predicted)
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- ?? ? ???? ?? (GHS)
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4-???-2,1,3-??????? C??? ??, ??, ??
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The Sonogashira cross-coupling reaction between 4-bromo-2, 1,3-benzothiadiazole, and the respective para-substituted phenylethynyl derivatives could synthesize the BTDs. In addition, the BTD-Ph is prepared by reacting 4-bromo-2,1,3-benzothiadiazole (Br-BTD)and palladium-MAI catalyst, and the dynamic phenylboronic acid reagent in the starting system or dynamic o-amino pyridine reagent[1-2].4-???-2,1,3-??????? ?? ?? ? ???
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4-???-2,1,3-??????? ?? ??
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4-???-2,1,3-??????? ?? ??:
4,7-DIBROMO-2,1,3-BENZOTHIADIAZOLE
4-bromo-2,1,3-benzothiadiazole
5-(BROMOMETHYL)-2,1,3-BENZOTHIADIAZOLE
5-BROMO-2,1,3-BENZOTHIADIAZOLE
2,1,3-Benzothiadiazole
7-BROMO-5-NITRO-2,1,3-BENZOTHIADIAZOL-4-AMINE
7-Bromo-2,1,3-benzothiadiazole-4-sulfonyl chloride
5-BROMO[1,2,5]THIADIAZOLO[3,4-E][2,1,3]BENZOXADIAZOLE 3-OXIDE
5,7-DIBROMO-2,1,3-BENZOTHIADIAZOL-4-AMINE
4-[(7-BROMO-5-NITRO-2,1,3-BENZOTHIADIAZOL-4-YL)THIO]-2-TERT-BUTYL-6-CHLOROQUINAZOLINE
6-[(7-BROMO-5-NITRO-2,1,3-BENZOTHIADIAZOL-4-YL)THIO]-7H-PURINE
7-BROMO-5-NITRO-4-PIPERIDIN-1-YL-2,1,3-BENZOTHIADIAZOLE
4-AZEPAN-1-YL-7-BROMO-5-NITRO-2,1,3-BENZOTHIADIAZOLE
7-BROMO-4-MORPHOLIN-4-YL-5-NITRO-2,1,3-BENZOTHIADIAZOLE
4,7-DIBROMO-5-NITRO-2,1,3-BENZOTHIADIAZOLE
4-[(7-BROMO-5-NITRO-2,1,3-BENZOTHIADIAZOL-4-YL)THIO]QUINAZOLINE
4-BROMO-2,1,3-BENZOTHIADIAZOL-5-AMINE
N-(4-BROMO-2,1,3-BENZOTHIADIAZOL-5-YL)-3-CHLORO-1-BENZOTHIOPHENE-2-CARBOXAMIDE