1727-39-5

Basic information

• Product Name: α-chloro β-phenyl acrylic acid
• Synonyms: α-chloro β-phenyl acrylic acid
• CAS NO: 1727-39-5
• Molecular Weight: 182.606
• Mol File: 1727-39-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: α-chloro β-phenyl acrylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: α-chloro β-phenyl acrylic acid(1727-39-5)
• EPA Substance Registry System: α-chloro β-phenyl acrylic acid(1727-39-5)

Safety Data

• Hazardous Substances Data: 1727-39-5(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 35115-76-5 2,3-dichloro-3-phenyl-propionic acid 
• 100-52-7 benzaldehyde 
• 79-11-8 chloroacetic acid 
• 62269-27-6 1-Chloro-2,2-difluoroethenyllithium 
• 23553-32-4 2-Chloro-2-[1,3]dioxolan-2-yl-1-phenyl-ethanol 
• 64-17-5 ethanol 
• 7782-50-5 chlorine 
• 4192-77-2 ethyl cinnamate 
• 359-10-4 1-Chloro-2,2-difluoroethene 
• 1727-31-7 (Z)-2-Chloro-3-phenyl-acrylic acid p-tolyl ester 
• 18365-42-9 α-chloro-cinnamaldehyde 
• 1733-33-1 2-Chlor-3-phenyl-acrylsaeure-phenylester 
• 3926-62-3 sodium monochloroacetic acid 

Downstream Products

• 708-86-1 α,β-dichloro-trans-cinnamic acid 
• 708-85-0 α,β-dichloro-cis-cinnamic acid 
• 637-44-5 phenylpropyolic acid 
• 827609-54-1 2,2,3-trichloro-3-phenyl-propionic acid 
• 56164-68-2 2,2,3-trichloro-3-phenyl-propionyl chloride 
• 56030-35-4 α-chloro-trans-cinnamic acid-chloride 
• 14737-94-1 methyl 2-chloro-3-phenylprop-2(Z)-enoate 
• 66051-36-3 ethyl (Z)-2-chloro-3-phenyl-2-propenoate 

Relevant articles and documents

Visible-light promoted oxidative cyclization of cinnamic acid derivatives using xanthone as the photocatalyst

We have developed an efficient photocatalytic synthesis of coumarin derivativesviaa tandem double bond isomerization/oxidative cyclization of cinnamic acids. Inexpensive and stable xanthone was used as the photocatalyst, and readily available Selectfluor was used as the oxidant. This method tolerates a wide range of functional groups and offers excellent chemical yields in general. Besides, the photocatalytic oxidative cyclization of cinnamic acid esters gives dimerized lignan-type products.