17684-15-0

Basic information

• Product Name: 3-(3-chlorophenyl)-3-phenylacrylic acid
• Synonyms: 3-(3-chlorophenyl)-3-phenylacrylic acid
• CAS NO: 17684-15-0
• Molecular Weight: 258.704
• Mol File: 17684-15-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(3-chlorophenyl)-3-phenylacrylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-chlorophenyl)-3-phenylacrylic acid(17684-15-0)
• EPA Substance Registry System: 3-(3-chlorophenyl)-3-phenylacrylic acid(17684-15-0)

Safety Data

• Hazardous Substances Data: 17684-15-0(Hazardous Substances Data)

Upstream product

• 1679-18-1 4-Chlorophenylboronic acid 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 134-85-0 4-chlorobenzophenone 
• 872269-68-6 ethyl 3-(4-chlorophenyl)-3-hydroxy-3-phenylpropanoate 
• 65565-13-1 3-(4-chlorophenyl)-3-hydroxy-3-phenylpropanoic acid 
• 64-19-7 acetic acid 
• 79-37-8 oxalyl dichloride 
• 18218-20-7 1-(4-chlorophenyl)-1-phenylethene 
• 1252576-58-1 ethyl (2Z)-3-(4-chlorophenyl)-3-phenylprop-2-enoate 
• 860582-56-5 C₁₇H₁₅ClO₂ 

Downstream Products

• 1437756-83-6 7-chloro-4-phenyl-2H-chromen-2-one 
• 1092835-45-4 4-(4-chlorophenyl)-2H-chromen-2-one 
• 1430119-20-2 (E)-1-chloro-4-(3,3,3-trifluoro-1-phenylprop-1-en-1-yl)benzene 
• 99632-23-2 (Z)-1-phenyl-1-(p-chlorophenyl)-2-bromoethylene 
• 99632-31-2 (E)-1-(2-bromo-1-phenylvinyl)-4-chlorobenzene 
• 612-00-0 1,1'-ethylidenebis-benzene 
• 606-83-7 3,3-Diphenylpropionic acid 
• 21998-30-1 3-(4-chlorophenyl)-3-phenylpropanoic acid 

Relevant articles and documents

Synthesis of coumarins via PIDA/I2-mediated oxidative cyclization of substituted phenylacrylic acids

A variety of functionalized coumarins were synthesized from substituted phenylacrylic acids via PIDA/I2-mediated and irradiation-promoted oxidative carbon-oxygen bond formation. Our studies show that the oxygen in the pendant carboxylic acid group cyclizes favorably to the aryl ring that is cis to it. The main advantages of this method include good functional group tolerance and the transition-metal-free characteristic. The Royal Society of Chemistry 2013.

Palladium-catalyzed intramolecular amidation of C(sp2)-H bonds: Synthesis of 4-aryl-2-quinolinones

Figure presented A catalytic synthetic approach for the synthesis of 2-quinolinone compounds through a Pd-catalyzed C(sp2)-H functionalization/intramolecular amidation sequence is described. The cyclization process efficiently proceeds in the p