5717-38-4

Basic information

• Product Name: Pentanoic acid, 2-(triphenylphosphoranylidene)-, ethyl ester
• Synonyms: 2-Triphenylphosphoranyliden-pentan-1-saeure-aethylester
• CAS NO: 5717-38-4
• Molecular Formula: C25H27O2P
• Molecular Weight: 390.462
• Mol File: 5717-38-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Pentanoic acid, 2-(triphenylphosphoranylidene)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Pentanoic acid, 2-(triphenylphosphoranylidene)-, ethyl ester(5717-38-4)
• EPA Substance Registry System: Pentanoic acid, 2-(triphenylphosphoranylidene)-, ethyl ester(5717-38-4)

Safety Data

• Hazardous Substances Data: 5717-38-4(Hazardous Substances Data)

Upstream product

• 107-08-4 1-iodo-propane 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 3728-50-5 butylidenetriphenylphosphorane 
• 541-41-3 chloroformic acid ethyl ester 

Downstream Products

• 5717-49-7 α-Propyl-γ,γ-diphenyl-allencarbonsaeure 
• 5717-46-4 ethyl 4,4-diphenyl-2-propyl-2,3-butadienoate 
• 894855-52-8 ethyl 4-phenyl-2-(n-propyl)-2,3-butadienoate 
• 130556-98-8 C₃₃H₂₇F₁₅NO₂P 
• 29304-46-9 2-Hydrocinnamoyl-n-valeriansaeure-aethylester 
• 2819-55-8 3-Oxo-6-phenyl-2-propyl-hexansaeure-aethylester 

Relevant articles and documents

Olefin-Directed Palladium-Catalyzed Regio- and Stereoselective Oxidative Arylation of Allenes

An olefin-directed palladium-catalyzed oxidative regio- and stereoselective arylation of allenes to afford 1,3,6-trienes has been established. A number of functionalized allenes, including 2,3- and 3,4-dienoates and 3,4-dienol derivatives, have been inves

VALPROIC ACID ANALOGUES AND PHARMACEUTICAL COMPOSITIONS THEREOF

Analogues of valproic acid useful in treating neuroaffective disorders including convulsions, bipolar disorder, and migraine headache are disclosed. The analogues are halide substituted analogues, cyclic analogues, and conjugated diene analogues of valproic acid. Pharmaceutical compositions or prodrugs containing the analogues or pharmaceutically acceptable salts thereof are disclosed. Methods of making the compounds and treating mammals with neuroaffective disorders are also disclosed.