76043-72-6

Basic information

• Product Name: 2,2-dichloro-3-phenylpropanoic acid
• Synonyms: 2,2-dichloro-3-phenylpropanoic acid
• CAS NO: 76043-72-6
• Molecular Weight: 219.067
• Mol File: 76043-72-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2,2-dichloro-3-phenylpropanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dichloro-3-phenylpropanoic acid(76043-72-6)
• EPA Substance Registry System: 2,2-dichloro-3-phenylpropanoic acid(76043-72-6)

Safety Data

• Hazardous Substances Data: 76043-72-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 39569-10-3 2-chloro-3-pentachloro-phenyl propenoic acid 
• 2136-78-9 α,α,2,3,4,5,6-pentachlorotoluene 
• 104-53-0 3-phenyl-propionaldehyde 
• 76043-69-1 2,2-dichloro-3-phenylpropionaldehyde 
• 1552-80-3 2,2-Dichlor-3-phenyl-propionsaeure-methylester 
• 79-43-6 dichloro-acetic acid 

Downstream Products

• 1309661-25-3 C₁₉H₁₈Cl₂N₂O₂ 
• 155088-09-8 N-Allyl-N-benzyl-2,2-dichloro-3-phenyl-propionamide 
• 155088-11-2 2,2-Dichloro-3-phenyl-propionyl chloride 

Relevant articles and documents

Total synthesis of (+)- and (-)-decursivine and (±)-serotobenine through a cascade witkop photocyclization/elimination/addition sequence: Scope and mechanistic insights

In this article, the total syntheses of antimalarial compound decursivine and its biologically inactive sibling serotobenine are presented. The biomimetic synthesis of (±)-serotobenine was investigated first, but failed. During the subsequent investigatio

Oxidation of aliphatic 2,2-dichloroalkanals by HNO3 in CH 2Cl2: An easy and eco-friendly route to the corresponding 2,2-dichloroalkanoic acids

A simple, economically convenient, and eco-compatible procedure for the oxidation of 2,2-dichloroalkanals to the corresponding alkanoic acids has been set up, employing HNO3 in CH2O2, in the presence of NaNO2 as catalyst.

Halogen atom transfer radical cyclization of N-allyl-N-benzyl-2,2-dihaloamides to 2-pyrrolidinones, promoted by Fe0-FeCl3 or CuCl-TMEDA

The halogen atom transfer radical cyclization of a N-allyl-N-benzyl-2,2-dihaloamides to 2-pyrrolidinones has been carried out in high yields under mild conditions, in a reaction promoted by CuCl-TMEDA or Fe0-FeCl3 in acetonitrile or N,N-dimethylformamide, respectively.