7379-67-1
7379-67-1
Chemical Structure
Iodobenzene-d5
Synonym(s): 1-Iodobenzene-d5
- CAS No.: 7379-67-1
- Formula:C6D5I
- Molecular Weight:209.04
IUPAC Name: ((1S,2R,5S)-8-((R)-1-phenylethyl)-8-azabicyclo[3.2.1]octan-2-yl)methanol hydrochloride
InChIKey: SNHMUERNLJLMHN-RALIUCGRSA-N
SMILES: IC1=C([2H])C([2H])=C([2H])C([2H])=C1[2H]
Biological Activity: 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[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
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. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
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. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
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]
Keywords
