CAS 6277-17-4
:2-iodo-1-methyl-3-nitrobenzene
Description:
2-Iodo-1-methyl-3-nitrobenzene is an organic compound characterized by the presence of an iodine atom, a methyl group, and a nitro group attached to a benzene ring. Its molecular structure features a benzene ring substituted at the 1-position with a methyl group, at the 2-position with an iodine atom, and at the 3-position with a nitro group, which contributes to its reactivity and properties. This compound is typically a yellow to brown solid at room temperature and is known for its moderate solubility in organic solvents. The presence of the nitro group makes it an electron-withdrawing group, influencing the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the iodine atom can participate in nucleophilic substitution reactions, making this compound useful in various synthetic applications in organic chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks and environmental hazards.
Formula:C7H6INO2
InChI:InChI=1/C7H6INO2/c1-5-3-2-4-6(7(5)8)9(10)11/h2-4H,1H3
SMILES:Cc1cccc(c1I)N(=O)=O
Synonyms:- Benzene, 2-iodo-1-methyl-3-nitro-
- 2-Iodo-1-methyl-3-nitrobenzene
- 2-Methyl-6-nitroiodobenzene
- 2-Iodo-3-nitrotoluene>
- 2-Iodo-3-methylnitrobenzene
- 2-Iodo-1-methyl-3-nitrotoluene
- 2-Iodo-1-methyl-3-nitro-benzene
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Found 5 products.
2-Iodo-1-methyl-3-nitrobenzene
CAS:Formula:C7H6INO2Purity:96%Color and Shape:SolidMolecular weight:263.03252-Iodo-3-nitrotoluene
CAS:2-Iodo-3-nitrotoluenePurity:≥95%Color and Shape:PowderMolecular weight:263.03g/mol2-Iodo-3-nitrotoluene
CAS:Formula:C7H6INO2Purity:>98.0%(GC)Color and Shape:Light orange to Yellow to Green powder to crystalMolecular weight:263.032-Iodo-1-methyl-3-nitrobenzene
CAS:<p>2-Iodo-1-methyl-3-nitrobenzene is an active compound that is used in chromatographic analysis. It has a high melting point and it is soluble in organic solvents. 2-Iodo-1-methyl-3-nitrobenzene can be used as a ligand to bind to nitrotoluene, which is then converted into biphenyl by the addition of amines and hydrochloric acid. 2-Iodo-1-methyl-3-nitrobenzene can be synthesized with a homochiral starting material, which produces an enantiomer with a chiral center. This reaction requires the use of thioethers and results in less than 5% yield.</p>Formula:C7H6INO2Purity:Min. 95%Color and Shape:PowderMolecular weight:263.03 g/mol




