1884-95-3

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 78-93-3 butanone 

Downstream Products

• 1202-60-4 3-(4-chlorophenyl)-3-methyl-2-acrylic acid 
• 75859-45-9 C₁₂H₁₅ClN₄ 
• 27932-61-2 (E)-5-(4-Chloro-phenyl)-4-methyl-1,1-bis-methylsulfanyl-penta-1,4-dien-3-one 
• 1101197-89-0 (S)-4-(4'-chlorophenyl)-3-methyl-butan-2-one 
• 1453502-17-4 (R)-4-(4'-chlorophenyl)-3-methyl-butan-2-one 
• 1879-52-3 cis-4-chloro-β-methylstyrene 

Relevant academic research and scientific papers

Enantiodivergence in the reduction of α-methyl and α-halomethyl enones by microorganisms

Enones (Z)-3-methyl-(Z)-3-chloromethyl- and (Z)-3-bromomethyl-4-R-3-buten- 2-one (R = n-pentyl, phenyl, 2′- and 4′-chlorophenyl, 3′- and 4′-nitrophenyl, 4′-methoxyphenyl) were synthesized and subjected to reduction by the microorganisms Saccharomyces cerevisiae andGeotrichum candidum. Whereas the bioreduction of 3-methy-4-R-3-buten-2-ones afforded the corresponding (S)-4-R-3-methybutan-2-ones, the bioreduction of 3-chloromethyl- and 3-bromomethyl-4-R-3-buten-2-ones afforded the corresponding (R)-4-R-3-methybutan-2-ones.

Room temperature aldol reactions using magnetic Fe3O 4@Fe(OH)3 composite microspheres in hydrogen bond catalysis

Fe3O4@Fe(OH)3 composite microspheres are highly active, environmentally friendly and easy to recycle catalysts for aldol reactions, which are catalyzed by a solid-liquid interfacial hydrogen bond catalyst at room temperature.