CAS 63452-69-7

Benzene, 1-iodo-4-methoxy-2-methyl-

Description:

Benzene, 1-iodo-4-methoxy-2-methyl-, also known by its CAS number 63452-69-7, is an aromatic organic compound characterized by a benzene ring substituted with an iodine atom, a methoxy group (-OCH3), and a methyl group (-CH3). This compound exhibits typical properties of aromatic compounds, including stability due to resonance and a relatively low reactivity compared to aliphatic compounds. The presence of the iodine substituent can enhance the electrophilic character of the benzene ring, making it more reactive towards electrophiles. The methoxy group is an electron-donating group, which can influence the compound's reactivity and solubility in various solvents. Additionally, the methyl group contributes to the overall hydrophobic character of the molecule. Benzene derivatives like this one are often used in organic synthesis and can serve as intermediates in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Safety considerations should be taken into account, as halogenated compounds can exhibit toxicity and environmental persistence.

Formula: C₈H₉IO

1-Iodo-4-methoxy-2-methylbenzene

CAS: 63452-69-7

Formula: C₈H₉IO

Purity: 96%

Color and Shape: Solid

Molecular weight: 248.0609

Ref: IN-DA00EL5P

1-Iodo-4-methoxy-2-methylbenzene

CAS: 63452-69-7

1-Iodo-4-methoxy-2-methylbenzene

Formula: C₈H₉IO

Purity: 96%

Color and Shape: off white to faint beige crystalline solid

Molecular weight: 248.06g/mol

Ref: 54-OR76325

1-Iodo-4-methoxy-2-methylbenzene

CAS: 63452-69-7

Purity: 96%

Color and Shape: Solid

Molecular weight: 248.0630035

Ref: 10-F628633

1-Iodo-4-methoxy-2-methylbenzene

CAS: 63452-69-7

1-Iodo-4-methoxy-2-methylbenzene (1IMMB) is an iodide which has been used as a precursor in the synthesis of carbonyl groups. This compound has also been shown to have high yields and mechanistic. The carbonyl group is located at the 1,3 positions and the methoxy group is located at the 2 position. This compound reacts with acetonitrile to form a naphthalene derivative. 1IMMB also reacts with an alcohol to form a cyclic ether with regiospecificity. It can also be used as a catalyst in the synthesis of unsymmetrical compounds that contain both carbonyl groups and alcohols.

Formula: C₈H₉IO

Purity: Min. 95%

Molecular weight: 248.06 g/mol

Ref: 3D-NCA45269