4'-Chloroacetophenone

CAS : 99-91-2

Ref. 3D-FC05532

Informations sur le produit

• Nom: 4'-Chloroacetophenone
• Synonymes: 1-(4-Chlorophenyl)-1-ethanone, 1-(4-Chlorophenyl)ethanone, 1-(p-Chlorophenyl)ethanone, 1-Acetyl-4-chlorobenzene, 1-Chloro-4-acetylbenzene, 4'-Chloracetophenon, 4'-Cloroacetofenona, 4-Acetyl-1-chlorobenzene, 4-Acetylchlorobenzene, 4-Acetylphenyl chloride, 4-Chloro-1-acetylbenzene, 4-Chlorobenzene methyl ketone, 4-Chlorohypnone, 4-Chlorophenyl methyl ketone, Acetophenone, 4'-chloro-, Acetophenone, p-chloro-, Methyl 4-chlorophenyl ketone, Methyl p-chlorophenyl ketone, Nsc 6115, P-Chloroacetophenone, p-Acetylchlorobenzene, p-Chlorohypnone, p-Chlorophenyl methyl ketone, Ethanone, 1-(4-chlorophenyl)-

Description

4'-Chloroacetophenone is a chemical substance that is used in the synthesis of other substances. It has been shown to be an effective tool for cell-specific reactions, such as methyl ketones and benzaldehyde. 4'-Chloroacetophenone reacts with hydrochloric acid and palladium complexes to produce electron reduction, which leads to the activation of methyl ketones. This reaction provides a method for synthesizing molecules with a carbonyl group. The isolated yield of this reaction is dependent on the reaction solution temperature and concentration. The mechanism of this reaction appears to be Suzuki coupling reaction.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 154.59 g/mol
• Formule: C₈H₇ClO
• Degré de pureté: Min. 95%
• Couleur/Forme: Clear Colourless To Pale Yellow Liquid
• InChI: InChI=1S/C8H7ClO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3
• Code InChI: InChIKey=BUZYGTVTZYSBCU-UHFFFAOYSA-N
• SMILES: CC(=O)c1ccc(Cl)cc1