CAS 13329-40-3

4-Iodoacetophenone

Description:

4-Iodoacetophenone is an organic compound characterized by its structure, which features an acetophenone moiety substituted with an iodine atom at the para position of the aromatic ring. This compound typically appears as a white to light yellow crystalline solid and is known for its moderate solubility in organic solvents such as ethanol and acetone, while being less soluble in water. It has a molecular formula of C9H9IO and a molecular weight that reflects the presence of iodine, which contributes to its unique reactivity and properties. 4-Iodoacetophenone is often utilized in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, due to its electrophilic nature, which allows it to participate in nucleophilic substitution reactions. Additionally, it can serve as a useful intermediate in the synthesis of other functionalized compounds. Safety precautions should be observed when handling this substance, as it may pose health risks if inhaled or ingested, and appropriate personal protective equipment should be used.

Formula: C₈H₇IO

InChI: InChI=1S/C8H7IO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3

InChI key: InChIKey=JZJWCDQGIPQBAO-UHFFFAOYSA-N

SMILES: C(C)(=O)C1=CC=C(I)C=C1

Synonyms:

• 1-(4-Iodofenil)Etan-1-Ona
• 1-(4-Iodophenyl)-1-ethanone
• 1-(4-Iodophenyl)Ethan-1-One
• 1-(4-Iodophenyl)Ethane-1-One
• 1-(4-Iodophenyl)ethanone
• 1-(4-Iodphenyl)ethan-1-on
• 1-Acetyl-4-iodobenzene
• 1-Iodo-4-acetylbenzene
• 4'-Iodoacetophenone
• 4-Acetyl-1-iodobenzene
• 4-Acetyliodobenzene
• 4-Acetylphenyl iodide
• 4-Iodophenyl methyl ketone
• Acetophenone, 4'-iodo-
• Acetophenone, p-iodo-
• Methyl 4-iodophenyl ketone
• Methyl p-iodophenyl ketone
• Nsc 97396
• p-Acetylphenyl iodide
• p-Iodoacetophenone
• p-Iodophenyl methyl ketone

4'-Iodoacetophenone

CAS: 13329-40-3

Formula: C₈H₇IO

Purity: >98.0%(GC)

Color and Shape: White to Yellow to Orange powder to crystal

Molecular weight: 246.05

Ref: 3B-I0305

4'-Iodoacetophenone, 98%

CAS: 13329-40-3

Synthesis of quinoline-based potential anticancer agents. Substrate for palladium-catalyzed coupling reactions This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original

Formula: C₈H₇IO

Purity: 98%

Color and Shape: Cream to yellow to orange to brown, Crystals or powder or crystalline powder

Molecular weight: 246.05

Ref: 02-A16794

Ethanone, 1-​(4-​iodophenyl)​-

CAS: 13329-40-3

Formula: C₈H₇IO

Purity: 98%

Color and Shape: Solid

Molecular weight: 246.0451

Ref: IN-DA0014JS

4'-Iodoacetophenone

CAS: 13329-40-3

4'-Iodoacetophenone

Formula: C₈H₇IO

Purity: 98%

Color and Shape: faint yellow powder

Molecular weight: 246.05g/mol

Ref: 54-OR7749

4′-Iodoacetophenone

CAS: 13329-40-3

Formula: C₈H₇IO

Purity: 98.0%

Color and Shape: Solid, Chunks or Crystalline Powder

Molecular weight: 246.047

Ref: 10-F003065

4'-Iodoacetophenone

CAS: 13329-40-3

4'-Iodoacetophenone is a catalyst in organic synthesis. It is a cross-coupling agent that is used to catalyze reactions of alkyl halides with organometallic compounds. The reaction mechanism is the same as for other cross-coupling reactions and involves the formation of a palladium complex. 4'-Iodoacetophenone has been shown to be effective in asymmetric synthesis, where it can be used as a homogeneous catalyst. This compound has also been shown to be an efficient methylating agent and can be used in the methylation of various functional groups, such as amines, nitro groups, and phenols.

Formula: C₈H₇IO

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 246.05 g/mol

Ref: 3D-FI55105