591-18-4
591-18-4
Chemical Structure
1-Bromo-3-iodobenzene
- CAS No.: 591-18-4
- Formula:C6H4BrI
- Molecular Weight:282.91
IUPAC Name: 1-bromo-3-iodobenzene
InChIKey: CTPUUDQIXKUAMO-UHFFFAOYSA-N
SMILES: IC1=CC(Br)=CC=C1
Biological Activity: 1-Bromo-3-iodobenzene is a biochemical reagent and an important organic synthetic intermediate. 1-Bromo-3-iodobenzene can be used for the synthesis of other active compounds[1][2].
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1-Bromo-3-iodobenzene | 99.99% | 1-Bromo-3-iodobenzene is a biochemical reagent and an important organic synthetic intermediate. 1-Bromo-3-iodobenzene can be used for the synthesis of other active compounds. | ||||||||||||||||||||
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1-Bromo-3-iodobenzene-d4 | 99.66% | 1-Bromo-3-iodobenzene-d4 is the deuterium labeled 1-Bromo-3-iodobenzene (HY-32149). 1-Bromo-3-iodobenzene is a biochemical reagent and an important organic synthetic intermediate. 1-Bromo-3-iodobenzene can be used for the synthesis of other active compounds. | ||||||||||||||||||||
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4-Bromo-2-fluoro-1-iodobenzene | 99.73% | 4-Bromo-2-fluoro-1-iodobenzene (4-Bromo-2-fluoroiodobenzene) is a halogenated aromatic building block and also serves as the starting material for the synthesis of the selective FGFR2 inhibitor LHQ766 (HY-180794). | ||||||||||||||||||||
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5-Bromo-2-iodopyridine | 5-Bromo-2-iodopyridine is a pyridine derivative containing bromine and iodine, which can be used in the synthesis of other active compounds, such as Lonafarnib. | |||||||||||||||||||||
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2-Bromo-5-iodopyridine | 96.39% | 2-Bromo-5-iodopyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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m-Iodophenol | 99.89% | m-Iodophenol is a protaetia brevitarsis attractant. | ||||||||||||||||||||
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1,4-Diiodobenzene | 99.88% | 1,4-Diiodobenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2-Bromo-4-iodopyridine | 2-Bromo-4-iodopyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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3-Bromofluorobenzene-13C6 | 3-Bromofluorobenzene-13C6 is the 13C labeled 3-Bromofluorobenzene. | |||||||||||||||||||||
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Iodobenzene | 99.91% | Iodobenzene can undergo Ullmann coupling reaction on copper catalyst to generate biphenyl. Iodobenzene can undergo Suzuki reaction with phenylboronic acid to generate biphenyl. | ||||||||||||||||||||
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References
- [1]. Diemer, et al. Efficient and Complementary Methods Offering Access to Synthetically Valuable 1, 2‐Dibromobenzenes. 2011: 327-340.
- [2]. Benmahdjoub S, et al. One-Pot Assembly of Unsymmetrical Biaryl Thioglycosides through Chemoselective Palladium-Catalyzed Three-Component Tandem Reaction. Org Lett. 2018 Jul 6;20(13):4067-4071. [Content Brief]
