398142-11-5

Basic information

• Product Name: 4-(4-chloro-phenyl)-4-pentenoic acid
• Synonyms: 4-(4-chloro-phenyl)-4-pentenoic acid
• CAS NO: 398142-11-5
• Molecular Weight: 210.66
• Mol File: 398142-11-5.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 4-(4-chloro-phenyl)-4-pentenoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-chloro-phenyl)-4-pentenoic acid(398142-11-5)
• EPA Substance Registry System: 4-(4-chloro-phenyl)-4-pentenoic acid(398142-11-5)

Safety Data

• Hazardous Substances Data: 398142-11-5(Hazardous Substances Data)

Upstream product

• 3984-34-7 4-(4-chlorophenyl)-4-oxobutanoic acid 
• 7148-01-8 methyl 4-(4-chlorophenyl)-4-oxobutanoate 
• 108-90-7 chlorobenzene 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 35804-44-5 ethyl 4-bromo-4-pentenoate 
• 92975-38-7 4-bromo-4-pentenoic acid tert-butyl ester 
• 1679-18-1 4-Chlorophenylboronic acid 
• 194805-62-4 methyl-4-bromo-pent-4-enoate 
• 118453-36-4 dimethyl 2-(2'-bromoallyl)malonate 

Downstream Products

• 1359975-46-4 2-(4-chlorophenyl)-2-methyl-tetrahydrofuran 
• 127590-48-1 1-(4-chlorophenyl)-4-hydroxy-1-butan-1-one 
• 89058-34-4 4-(4-chlorophenyl)pent-4-enal 
• 21034-35-5 5-(4-chlorophenyl)-5-methyldihydrofuran-2(3H)-one 

Relevant articles and documents

Synthesis of Novel C 2-Symmetric Sulfur-Based Catalysts: Asymmetric Formation of Halo- and Seleno-Functionalized Normal- and Medium-Sized Rings

The synthesis of novel, highly functionalized, C 2 -symmetric sulfur-based catalysts is developed and their catalytic applications are explored in asymmetric bromo-, iodo- and seleno-functionalizations of alkenoic acids. This protocol provides

Visible-Light-Catalyzed Phosphonation-Annulation: an Efficient Strategy to Synthesize β-Phosphonopyrrolidines and β-Phosphonolactones

A new type of phosphine radical precursor for C—P bond formation has been developed and successfully used in visible-light-catalyzed phosphonation-annulation of unsaturated sulfonamides and carboxylic acids. The catalytic process is simple and green acces

Photoredox-Catalyzed Cascade Difluoroalkylation and Intramolecular Cyclization for Construction of Fluorinated γ-Butyrolactones

A cascade visible-light photocatalytic difluoroalkylation and intramolecular cyclization reaction has been developed for the synthesis of difluoroalkylated oxygen heterocycles. The reaction was carried out under very mild conditions, affording fluorinated