CAS 1023-17-2

4'-METHOXY-2-PHENYLACETOPHENONE

Description:

4'-Methoxy-2-phenylacetophenone, with the CAS number 1023-17-2, is an organic compound that belongs to the class of ketones and is characterized by its aromatic structure. It features a methoxy group (-OCH3) and two phenyl rings, which contribute to its stability and reactivity. This compound is often utilized as a photoinitiator in polymer chemistry, particularly in UV-curable systems, due to its ability to absorb UV light and initiate polymerization processes. Its molecular structure allows for effective light absorption, making it valuable in coatings, inks, and adhesives. Additionally, 4'-methoxy-2-phenylacetophenone exhibits moderate solubility in organic solvents, which enhances its applicability in various formulations. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks upon exposure. Overall, its unique chemical properties and functional groups make it a significant compound in industrial applications, particularly in the field of materials science.

Formula: C₁₅H₁₄O₂

InChI: InChI=1/C15H14O2/c1-17-14-9-7-13(8-10-14)15(16)11-12-5-3-2-4-6-12/h2-10H,11H2,1H3

SMILES: COc1ccc(cc1)C(=O)Cc1ccccc1

Synonyms:

• 4-Methoxyphenylbenzyl Ketone
• Deoxy-4-Methoxybenzoin
• Benzyl 4-Methoxyphenyl Ketone
• Nsc26658
• 1-(4-Methoxyphenyl)-2-Phenylethanone
• 1-(4-Methoxyphenyl)acetophenone

Ethanone, 1-(4-methoxyphenyl)-2-phenyl-

CAS: 1023-17-2

Formula: C₁₅H₁₄O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 226.2705

Ref: IN-DA00075Z

4'-Methoxy-2-phenylacetophenone

CAS: 1023-17-2

4'-Methoxy-2-phenylacetophenone

Purity: 98%

Molecular weight: 226.27g/mol

Ref: 54-OR4803

1-(4-Methoxyphenyl)-2-phenylethanone

CAS: 1023-17-2

Formula: C₁₅H₁₄O₂

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 226.28

Ref: 3B-M3551

1-(4-Methoxyphenyl)acetophenone

CAS: 1023-17-2

1-(4-Methoxyphenyl)acetophenone is an enantiomer of the naturally occurring compound melatonin. It has been shown to have insecticidal activities and is effective against insects at temperatures below 10°C. 1-(4-Methoxyphenyl)acetophenone undergoes a cyclodehydration reaction with loss of water and formation of a six-membered ring, which is catalysed by acid, inorganic bases, or metal salts. This reaction can be modified by substituting diacids, halides, or electrolysing agents for water. The resulting products are unsymmetrical and soluble in organic solvents.

Formula: C₁₅H₁₄O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 226.27 g/mol

Ref: 3D-FM25326

4′-Methoxy-2-phenylacetophenone

CAS: 1023-17-2

Formula: C₁₅H₁₄O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 226.275

Ref: 10-F022860

1-(4-Methoxyphenyl)acetophenone

Controlled Product

CAS: 1023-17-2

Applications An intermediate for the synthesis of many biologically active molecules including receptor ligands and enzyme inhibitors
References Chesworth, R., et al.: Bioorg. Med. Chem. Lett., 15, 5562 (2005), Gupta, A., et al.: Med. Chem., 3, 241 (2007), Ramajayam, R., et al.: Eur. J. Med. Chem., 43, 2004 (2008),

Formula: C₁₅H₁₄O₂

Color and Shape: Neat

Molecular weight: 226.27

Ref: TR-M265800