117896-34-1

Basic information

• Product Name: 1-(4-fluorobenzyl)-2-methoxybenzene
• Synonyms: 1-(4-fluorobenzyl)-2-methoxybenzene
• CAS NO: 117896-34-1
• Molecular Weight: 216.255
• Mol File: 117896-34-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(4-fluorobenzyl)-2-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-fluorobenzyl)-2-methoxybenzene(117896-34-1)
• EPA Substance Registry System: 1-(4-fluorobenzyl)-2-methoxybenzene(117896-34-1)

Safety Data

• Hazardous Substances Data: 117896-34-1(Hazardous Substances Data)

Upstream product

• 83724-41-8 tris(2-methoxyphenyl)bismuthine 
• 352-11-4 1-chloromethyl-4-fluorobenzene 
• 502-00-1 p-fluorobenzyl acetate 
• 100-66-3 methoxybenzene 
• 16750-63-3 2-methoxyphenylmagnesium bromide 
• 459-57-4 4-fluorobenzaldehyde 
• 124937-80-0 (4-fluorophenyl)(2-methoxyphenyl)methanol 

Downstream Products

• 117917-24-5 (S)-3-{4-[3-(4-Fluoro-benzyl)-4-methoxy-phenoxy]-3,5-diiodo-phenyl}-2-(2,2,2-trifluoro-acetylamino)-propionic acid methyl ester 
• 117653-11-9 (S)-2-Amino-3-{4-[3-(4-fluoro-benzyl)-4-hydroxy-phenoxy]-3,5-diiodo-phenyl}-propionic acid 

Relevant articles and documents

Threefold and chemoselective couplings of triarylbismuths with benzylic chlorides and iodides using palladium catalysis

This paper describes the palladium-catalyzed studies on threefold coupling of triarylbismuth reagents with benzylic chlorides and iodides. The optimized protocol conditions are operationally simple, delivering threefold coupling of a variety of triarylbismuths in combination with benzylic chlorides and iodides. The two optimized protocols allowed the synthesis of a diverse range of unsymmetrical diarylmethanes in an efficient manner. As part of this study, chemoselective transformation of benzylic chlorides and iodides was also achieved. This journal is the Partner Organisations 2014.

3,3-DIPHENYLPROPYLAMINES AND PHARMACEUTICAL COMPOSITIONS THEREOF

Novel 3,3-diphenylpropylamines of formula (I) wherein R1 signifies hydrogen or methyl, R2, R3 and R4 independently signify hydrogen, methyl, methoxy, hydroxy, carbamoyl, sulphanoyl or halogen, and X represents a tertiary amino group -NR5, R6, wherein R5 and R6 signify non-aromatic hydrocarbyl groups, which may be the same or different and which together contain at least three carbon atoms, and which may form a ring together with the amine nitrogen, their salts with physiologically acceptable acids and, when the compounds can be in the form of optical isomers, the racemic mixture and the individual enantiomers, their use as drugs, especially as anticholinergic agents, their use for preparing an anticholinergic drug, pharmaceutical compositions containing the novel amines, and methods for preparing the same