141478-00-4

Basic information

• Product Name: Chlorure de l' acide diphenyl-4,4 butyrique
• Synonyms: Chlorure de l' acide diphenyl-4,4 butyrique
• CAS NO: 141478-00-4
• Molecular Weight: 258.748
• Mol File: 141478-00-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Chlorure de l' acide diphenyl-4,4 butyrique(CAS DataBase Reference)
• NIST Chemistry Reference: Chlorure de l' acide diphenyl-4,4 butyrique(141478-00-4)
• EPA Substance Registry System: Chlorure de l' acide diphenyl-4,4 butyrique(141478-00-4)

Safety Data

• Hazardous Substances Data: 141478-00-4(Hazardous Substances Data)

Upstream product

• 14578-67-7 4,4-diphenylbutanoic acid 
• 1008-76-0 4,5-dihydro-5-phenyl-2(3H)-furanone 
• 71-43-2 benzene 

Downstream Products

• 1111702-40-9 N-(4,4-diethoxybutyl)-4,4-diphenyl-butyramide 
• 94743-24-5 3-(2,3-Dimethyl-phenyl)-1-[1-(2,2-diphenyl-ethyl)-3,3-dimethyl-2-oxo-butyl]-1H-quinazoline-2,4-dione 
• 94743-41-6 4-Bromo-2,2-dimethyl-6,6-diphenyl-hexan-3-one 
• 14578-68-8 4-phenyl-3,4-dihydronaphthalen-1(2H)-one 
• 141477-88-5 4,4-Diphenyl-butyric acid 4-methyl-morpholin-2-yl ester 
• 94743-28-9 2,2-Dimethyl-6,6-diphenyl-hexan-3-one 
• 1047663-46-6 N-hydroxy-N-phenyl-4,4-diphenylbutyramide 

Relevant articles and documents

A facile synthesis of pyrrolo-(di)-benzazocinones via an intramolecular N-acyliminium ion cyclisation

A facile, moderate to high yielding synthesis of hexahydro-(di)- benzazocinones is described via an intramolecular N-acyliminium ion cyclisation. The iminium ion intermediates are formed from the readily available 4,4-diethoxybutyl amides with an excess of triflic acid. For electron-withdrawing substituents, better yields were obtained from the pre-formed 2-hydroxypyrrolidine amides. From NMR studies, at ambient temperatures the pyrrolo-benzazocin-3-ones exist as a slowly equilibrating mixture of two conformations.

The synthesis and antilipidperoxidation activity of 4,4-diarylbutylamines and 4,4-diarylbutanamides

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