116941-51-6

Basic information

• Product Name: 1,1':3',1''-Terphenyl, 4-chloro-5'-phenyl-
• Synonyms: 1,1':3',1''-Terphenyl, 4-chloro-5'-phenyl-;4-chloro-5'-phenyl-1,1':3',1''-Terphenyl
• CAS NO: 116941-51-6
• Molecular Formula: C₂₄H₁₇Cl
• Molecular Weight: 340.84478
• Mol File: 116941-51-6.mol
• Article Data: 10

Chemical Properties

• Melting Point: 141.0 to 145.0 °C
• Boiling Point: 489.9±14.0 °C(Predicted)
• Appearance: /
• Density: 1.146±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,1':3',1''-Terphenyl, 4-chloro-5'-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1':3',1''-Terphenyl, 4-chloro-5'-phenyl-(116941-51-6)
• EPA Substance Registry System: 1,1':3',1''-Terphenyl, 4-chloro-5'-phenyl-(116941-51-6)

Safety Data

• Hazardous Substances Data: 116941-51-6(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 872789-01-0 [6-(4-chloro-phenyl)-2-hydroxy-2,4-diphenyl-cyclohex-3-enyl]-phenyl ketone 
• 108-24-7 acetic anhydride 
• 495-45-4 dypnone 
• 99-91-2 para-chloroacetophenone 
• 54435-79-9 (E)-1,3-diphenyl-3-methyl-2-propen-1-one 
• 13301-77-4 3-bromo-3-(4-chlorophenyl)acrylaldehyde 
• 35491-57-7 (E,Z)-2-benzoyl-3-phenylbut-2-enenitrile 
• 22966-22-9 (E)-1-(4-chlorophenyl)-3-phenyl-2-propen-1-one 
• 67-68-5 dimethyl sulfoxide 
• 1222-98-6 4-nitrochalcone 
• 98124-35-7 4-nitro-[1,1':3',1-terphenyl]-5'-phenol 
• 3816-12-4 4'-nitro-5'-phenyl-1,1':3',1''-terphenyl 
• 343239-58-7 5′-phenyl-[1,1′:3′,1″-terphenyl]-4-amine 
• 555-16-8 4-nitrobenzaldehdye 

Relevant articles and documents

Synthesis of asymmetric triarylbenzenes by using SOCl2-C 2H5OH reagent

A simple and efficient method for synthesis of asymmetric branched functionalized triarylbenzenes is presented. The dypnone reacting with different substituted acetophenones, corresponding asymmetric 1,3,5-triarylbenzenes were obtained in the presence of catalytic amounts of sulfurous oxychloride in anhydrous ethanol.

N-Heterocyclic Carbene-Catalyzed Construction of 1,3,5-Trisubstituted Benzenes from Bromoenals and α-Cyano-β-methylenones

A direct and efficient approach to 1,3,5-trisubstituted benzenes has been developed via N-heterocyclic carbene-catalyzed [2 + 4] annulation of α-bromoenals and α-cyano-β-methylenones. The reaction worked well for both aryl- and alkylenones.

A halogen substituted of compounds of preparation method

The invention discloses a type 1 shown compound preparation method, comprises the following steps: (1) condensation reaction: (2) Cyclization reaction: (3) The substitution reaction: (4) Coupling reaction: (5) Reduction reaction: (6) The diazotization reaction: Wherein X is selected from F, Cl, Br, I.