CAS 214279-40-0

2-iodo-4-methoxy-1-nitrobenzene

Description:

2-Iodo-4-methoxy-1-nitrobenzene is an organic compound characterized by its aromatic structure, which includes a nitro group (-NO2), an iodo group (-I), and a methoxy group (-OCH3) attached to a benzene ring. The presence of these substituents influences its chemical reactivity and physical properties. The iodo group typically enhances the compound's electrophilicity, making it more reactive in nucleophilic substitution reactions. The methoxy group, being an electron-donating group, can stabilize the aromatic ring and influence the orientation of further substitutions. The nitro group is a strong electron-withdrawing group, which can affect the acidity and reactivity of the compound. In terms of solubility, 2-iodo-4-methoxy-1-nitrobenzene is likely to be soluble in organic solvents due to its non-polar aromatic nature, while its polar functional groups may impart some degree of solubility in polar solvents. This compound can be utilized in various synthetic applications, particularly in the field of medicinal chemistry and materials science.

Formula: C₇H₆INO₃

InChI: InChI=1/C7H6INO3/c1-12-5-2-3-7(9(10)11)6(8)4-5/h2-4H,1H3

SMILES: COc1ccc(c(c1)I)N(=O)=O

Synonyms:

• 3-Iodo-4-nitroanisole

3-Iodo-4-Nitroanisole

CAS: 214279-40-0

Formula: C₇H₆INO₃

Purity: 96%

Color and Shape: Solid

Molecular weight: 279.0319

Ref: IN-DA00C1WX

3-Iodo-4-nitroanisole

CAS: 214279-40-0

3-Iodo-4-nitroanisole

Formula: C₇H₆INO₃

Purity: 98%

Color and Shape: beige/yellow powder

Molecular weight: 279.03g/mol

Ref: 54-OR13079

4-Nitro-3-iodoanisole

CAS: 214279-40-0

4-Nitro-3-iodoanisole is a bauerine that is used as a ligand in asymmetric catalysis. It is an atropisomeric compound, meaning it can exist in two different forms. The two forms of 4-nitro-3-iodoanisole are identical except for the orientation of the axial ligands on opposite sides of the molecule. The axial ligands on one form are biphenyl and nitrous oxide, while the axial ligands on the other form are nitrous oxide and biphenyl. 4-Nitro-3-iodoanisole has been used to catalyze reactions such as alkylation and coupling reactions with a variety of substrates, including β-carbolines, phenols, and amines.

Formula: C₇H₆INO₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 279.03 g/mol

Ref: 3D-FN67687

2-Iodo-4-methoxy-1-nitrobenzene

CAS: 214279-40-0

Formula: C₇H₆INO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 279.033

Ref: 10-F321618