CAS 20442-79-9
:3-Iodobiphenyl
Description:
3-Iodobiphenyl is an organic compound characterized by the presence of an iodine atom attached to the third position of a biphenyl structure, which consists of two phenyl rings connected by a single bond. This compound is typically a white to light yellow solid at room temperature and is known for its aromatic properties. It is relatively insoluble in water but soluble in organic solvents such as ethanol and dichloromethane. 3-Iodobiphenyl is used in various applications, including organic synthesis, as a building block in the preparation of pharmaceuticals, agrochemicals, and materials science. The presence of the iodine atom enhances its reactivity, making it useful in electrophilic substitution reactions and cross-coupling reactions, such as Suzuki and Stille reactions. Additionally, 3-iodobiphenyl can serve as a precursor for the synthesis of other functionalized biphenyl derivatives. As with many halogenated compounds, it is important to handle 3-iodobiphenyl with care due to potential health and environmental impacts.
Formula:C12H9I
InChI:InChI=1S/C12H9I/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H
InChI key:InChIKey=KAQUBIATNWQNRE-UHFFFAOYSA-N
SMILES:IC=1C=C(C=CC1)C2=CC=CC=C2
Synonyms:- 1,1'-Biphenyl, 3-iodo-
- 1-Iodo-3-phenylbenzene
- 3-Biphenyl iodide
- 3-Iodo-Biphenyl
- 3-Iodobiphenyl
- Biphenyl, 3-iodo-
- m-Iodobiphenyl
- 3-Iodo-1,1′-biphenyl
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Found 6 products.
3-Iodobiphenyl
CAS:Formula:C12H9IPurity:>98.0%(GC)Color and Shape:Light orange to Yellow to Green clear liquidMolecular weight:280.111,1'-Biphenyl, 3-iodo-
CAS:<p>1,1'-Biphenyl, 3-iodo- is a bioactive chemical.</p>Formula:C12H9IColor and Shape:SolidMolecular weight:280.103-Iodobiphenyl
CAS:<p>3-Iodobiphenyl is a synthetic chemical compound that has been used in the manufacture of dyes, pesticides, and other organic chemicals. 3-Iodobiphenyl is a low molecular weight soluble solid with a high solubility in most organic solvents. It is insoluble in water and may be produced as one of two different isomeric forms, depending on the conditions used to synthesize it. The physical properties of these two forms are similar but they differ in their reactivity. 3-Iodobiphenyl can adsorb onto amine groups on proteins and phospholipid membranes, forming a monolayer that alters the permeability of membrane bilayers. This organocatalytic reaction can also be facilitated by metal ions such as copper or zinc. 3-Iodobiphenyl also reacts with halides such as chloride or bromide to form soluble complexes that may be used for solute separation during phase chrom</p>Formula:C12H9IPurity:Min. 95%Molecular weight:280.11 g/mol





