ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Pyridine compound > Bromopyridine > 3,4-Dibromopyridine
3,4-Dibromopyridine
3,4-Dibromopyridine Basic information
- Product Name:
- 3,4-Dibromopyridine
- Synonyms:
-
- SPECS AC-907/25004343
- 3,4-DIBROMOPYRIDINE
- 3,4-Dibromopyridine98%
- Pyridine, 3,4-dibromo-
- 3,4-DIBROMOPYRIDINE ISO 9001:2015 REACH
- 4-DIBROMOPYRIDINE
- CAS:
- 13534-90-2
- MF:
- C5H3Br2N
- MW:
- 236.89
- EINECS:
- 800-799-3
- Product Categories:
-
- Pyridine
- pharmacetical
- Pyridines
- Brominated heterocyclic series
- Mol File:
- 13534-90-2.mol
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3,4-Dibromopyridine Chemical Properties
- Melting point:
- 71-72 C
- Boiling point:
- 239.9±20.0 °C(Predicted)
- Density
- 2.059±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- 2.06±0.10(Predicted)
- form
- powder to crystal
- color
- White to Yellow to Orange
- CAS DataBase Reference
- 13534-90-2(CAS DataBase Reference)
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3,4-Dibromopyridine Usage And Synthesis
Uses
3,4-dibromopyridine is a vital organic compound that could synthesise virous azaindoles. 6-Azaindoles are formed through site-selective Pd-catalyzed Sonogashira reaction of 3,4-dibromopyridine with alkynes, followed by a Pd-catalyzed tandem C–N coupling and cyclization with amines. On the other hand, 5-azaindoles are obtained by a site-selective Pd-catalyzed C–N coupling reaction of 3,4-dibromopyridine with amines, followed by C–C coupling and cyclization with alkynes[1].
References
[1] N. Son. “Synthesis of 5- and 6-Azaindoles by Sequential Site-Selective Palladium-Catalyzed C–C and C–N Coupling Reactions.” Synlett 52 1 (2020): 1308–1312.
3,4-DibromopyridineSupplier
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3,4-Dibromopyridine(13534-90-2)Related Product Information
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- 3-Amino-2,6-dibromopyridine ,98%
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- 3,5-DIBROMOPYRIDINE 1-OXIDE,3,5-DIBROMOPYRIDINE-PYRIDIN 1-OXIDE, 98+%