591-50-4
591-50-4
Chemical Structure
Iodobenzene
Synonym(s): 1-Iodobenzene
- CAS. Nr.: 591-50-4
- Formula:C6H5I
- Molecular Weight:204.01
IUPAC Name: iodobenzene
InChIKey: SNHMUERNLJLMHN-UHFFFAOYSA-N
SMILES: IC1=CC=CC=C1
Biological Activity: Iodobenzene can undergo Ullmann coupling reaction on copper catalyst to generate biphenyl. Iodobenzene can undergo Suzuki reaction with phenylboronic acid to generate biphenyl[1][2].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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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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Iodobenzene-d5 | 99.52% | Iodobenzene-d5 is the deuterium labeled 1-Iodobenzene. 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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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-Fluoro-2-iodobenzene | 99.43% | 1-Fluoro-2-iodobenzene 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-Iodoaniline | 99.97% | 2-Iodoaniline (2-Iodophenylamine) is an aniline derivative, and has potential hepatotoxic and nephrotoxic activity. | ||||||||||||||||||||
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2-Iodoaniline-13C6 | 2-Iodoaniline-13C6 is the 13C labeled 2-Iodoaniline. | |||||||||||||||||||||
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m-Iodophenol | 99.89% | m-Iodophenol is a protaetia brevitarsis attractant. | ||||||||||||||||||||
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Tropone | 97.80% | Tropone (Cycloheptatrienone) is a non-benzenoid aromatic natural product that acts as a membrane reverse transporter and metal chelator. Tropone disrupts the proton motive force by affecting the transmembrane proton gradient and functions as a quorum sensing signal through LuxR-type transcriptional regulators. Tropone exhibits broad-spectrum antibiotic, anticancer, algicidal, and probiotic activities. As a virulence factor toxic to rice seedlings, Tropone promotes biofilm formation in Burkholderia plantarii and induces neurotoxicity involving mitochondrial and cytoskeletal damage, increased Ca2+ influx, and oxidative stress. Tropone is used in the study of bacterial infections. | ||||||||||||||||||||
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Phenol, potassium salt (4:1) | Phenol, potassium salt (4:1) is a metal-organic framework (MOF). | |||||||||||||||||||||
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References
- [1]. Xi M, et al. Iodobenzene on Cu (111): formation and coupling of adsorbed phenyl groups[J]. Surface science, 1992, 278(1-2): 19-32.
- [2]. Narayanan R, et al. Effect of catalysis on the stability of metallic nanoparticles: Suzuki reaction catalyzed by PVP-palladium nanoparticles. J Am Chem Soc. 2003 Jul 9;125(27):8340-7. [Content Brief]
