1444122-30-8

Basic information

• Product Name: 1-(4-butyl-1,1':3',1''-terphenyl-5'-yl)naphthalene
• Synonyms: 1-(4-butyl-1,1':3',1''-terphenyl-5'-yl)naphthalene
• CAS NO: 1444122-30-8
• Molecular Weight: 412.574
• Mol File: 1444122-30-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-butyl-1,1':3',1''-terphenyl-5'-yl)naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-butyl-1,1':3',1''-terphenyl-5'-yl)naphthalene(1444122-30-8)
• EPA Substance Registry System: 1-(4-butyl-1,1':3',1''-terphenyl-5'-yl)naphthalene(1444122-30-8)

Safety Data

• Hazardous Substances Data: 1444122-30-8(Hazardous Substances Data)

Upstream product

• 1444122-63-7 3-hydroxy-5-methoxyphenyl tosylate 
• 1444121-90-7 3-(diethylcarbamoyloxy)-5-methoxyphenyl tosylate 
• 1444121-92-9 3-(diethylcarbamoyloxy)-5-methoxybiphenyl 
• 2174-64-3 5-methoxyresorcinol 
• 1444122-03-5 5'-methoxy-4-methyl-1,1':3',1''-terphenyl 
• 185416-14-2 4-(1-butyl)phenylmagnesium bromide 
• 1444122-57-9 5-methoxy-1,3-phenylene dipivalate 
• 1444122-59-1 3-hydroxy-5-methoxyphenyl pivalate 
• 1444122-61-5 3-methoxy-5-(tosyloxy)phenyl pivalate 

Relevant articles and documents

Programmed selective sp2 C-O bond activation toward multiarylated benzenes

A variety of important multiarylated benzenes were efficiently synthesized from phloroglucinol derivatives 1 through sequential cross-couplings via Pd-catalyzed C-OTs, Ni-catalyzed C-OC(O)NEt2, and C-OMe bond activation. High selectivity was achieved based on the rational design and inherent diversity in the reactivity of different C-O bonds.