CAS 25245-27-6

Benzene,1-iodo-3,5-dimethoxy-

Description:

Benzene, 1-iodo-3,5-dimethoxy- is an organic compound characterized by its aromatic benzene ring substituted with iodine and two methoxy groups at the 3 and 5 positions. This compound typically appears as a colorless to pale yellow liquid and is known for its distinct aromatic odor. The presence of the iodine atom introduces notable reactivity, particularly in nucleophilic substitution reactions, while the methoxy groups can influence the compound's electronic properties and solubility. The methoxy groups are electron-donating, which can enhance the reactivity of the aromatic system. This compound is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Due to the presence of iodine, it may also exhibit some level of toxicity and should be handled with care in a controlled laboratory environment. Proper safety measures, including the use of personal protective equipment, are essential when working with this substance.

Formula: C₈H₉IO₂

Synonyms:

• 1,3-Dimethoxy-5-iodobenzene
• 1-Iodo-3,5-dimethoxybenzene
• 3,5-Dimethoxy-1-iodobenzene
• 3,5-Dimethoxyiodobenzene
• 3,5-Dimethoxyphenyl iodide

1-Iodo-3,5-dimethoxybenzene

CAS: 25245-27-6

Formula: C₈H₉IO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 264.0603

Ref: IN-DA00BDQY

1-Iodo-3,5-dimethoxybenzene

CAS: 25245-27-6

1-Iodo-3,5-dimethoxybenzene

Formula: C₈H₉IO₂

Purity: 95%

Color and Shape: yellow solid

Molecular weight: 264.06g/mol

Ref: 54-OR72102

1,3-Dimethoxy-5-iodobenzene

CAS: 25245-27-6

Formula: C₈H₉IO₂

Molecular weight: 264.06

Ref: 7W-GX7393

3,5-Dimethoxyiodobenzene

Controlled Product

CAS: 25245-27-6

Applications Intermediate for the synthesis of glucuronide conjugates of trans-Resveratrol
References Kitagawa, M., et al.: Chem. Pharm. Bull., 39, 2681 (1991), Keller, T., et al.: Chem. Pharm. Bull., 49, 1009 (2001),

Formula: C₈H₉IO₂

Color and Shape: Neat

Molecular weight: 264.06

Ref: TR-D460640

3,5-Dimethoxyiodobenzene

CAS: 25245-27-6

3,5-Dimethoxyiodobenzene is an organic molecule that is structurally similar to biphenyl. It has been shown to inhibit the growth of cancer cells by flipping the mcf-7 protein and cross-coupling with pterostilbene. 3,5-Dimethoxyiodobenzene can be used as a substitute for biphenyl in some reactions because it has a similar structure but does not have halogen groups. 3,5-Dimethoxyiodobenzene also inhibits the production of chloride ions in bacteria and causes accumulation of phosphane, which is an enzyme inhibitor. This compound has also been shown to act as a stereoselective inhibitor of enzymes that catalyze the synthesis of phytoalexins, which are plant secondary metabolites produced under biotic stress conditions (e.g., bacterial infection).

Formula: C₈H₉IO₂

Purity: Min. 95%

Color and Shape: Light Brown To Brown Solid

Molecular weight: 264.06 g/mol

Ref: 3D-FD22205

1,3-Dimethoxy-5-iodobenzene

CAS: 25245-27-6

Formula: C₈H₉IO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 264.062

Ref: 10-F050463