113541-07-4

Basic information

• Product Name: Ethanone, 1,2-bis(2,4-dichlorophenyl)-2-hydroxy-
• CAS NO: 113541-07-4
• Molecular Formula: C14H8Cl4O2
• Molecular Weight: 350.028
• Mol File: 113541-07-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 1,2-bis(2,4-dichlorophenyl)-2-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1,2-bis(2,4-dichlorophenyl)-2-hydroxy-(113541-07-4)
• EPA Substance Registry System: Ethanone, 1,2-bis(2,4-dichlorophenyl)-2-hydroxy-(113541-07-4)

Safety Data

• Hazardous Substances Data: 113541-07-4(Hazardous Substances Data)

Upstream product

• 874-42-0 2,4-dichlorobenzaldeyhde 
• 104-88-1 4-chlorobenzaldehyde 
• 77287-34-4 formamide 

Downstream Products

• 1372399-27-3 2,3-di(2,4-dichlorophenyl)quinoxaline 
• 1615691-60-5 (4S,5S)-5-(2,4-dichlorobenzoyl)-5-(2,4-dichlorophenyl)-4-phenyldihydrofuran-2(3H)-one 
• 489447-35-0 4,5-di-(2,4-dichlorophenyl)oxazole 
• 489447-40-7 (+/-)-4'-chloro-2-hydroxy-2-(2,4-dichlorophenyl)acetophenone 
• 94171-15-0 2-(2,4-dichlorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-2',4'-dichloropropiophenone 
• 94147-83-8 2-(2,4-dichlorobenzoyl)-2-(2,4-dichlorophenyl)oxirane 
• 107680-38-6 Toluene-4-sulfonic acid 2,3-bis-(2,4-dichloro-phenyl)-2-hydroxy-3-oxo-propyl ester 
• 107659-73-4 (4S,5R)-4,5-Bis-(2,4-dichloro-phenyl)-4-[1,2,4]triazol-1-ylmethyl-[1,3]dioxolan-2-one 
• 107659-45-0 (1R,2S)-1,2-Bis-(2,4-dichloro-phenyl)-3-[1,2,4]triazol-1-yl-propane-1,2-diol 
• 94146-95-9 1,2-Bis-(2,4-dichloro-phenyl)-2-hydroxy-3-[1,2,4]triazol-4-yl-propan-1-one 
• 94171-12-7 1,2-Bis-(2,4-dichloro-phenyl)-2-hydroxy-3-imidazol-1-yl-propan-1-one 
• 94146-88-0 (1S,2R)-1,2-Bis-(4-chloro-phenyl)-3-imidazol-1-yl-propane-1,2-diol 
• 107680-37-5 1,2-Bis-(2,4-dichloro-phenyl)-2,3-dihydroxy-propan-1-one 

Relevant articles and documents

Synthesis of functionalized γ-lactones via a three-component cascade reaction catalyzed by consecutive N-heterocyclic carbene systems

Two consecutive N-heterocyclic carbene (NHC) catalytic systems were combined in a one-pot cascade reaction for the assembly of aromatic aldehydes and 2-haloenals into a structurally complex γ-lactone backbone. To our knowledge, this is the first report of NHC-catalyzed [3 + 2] annulation of α,β-unsaturated acylazoliums with 1,2-bisnucleophiles.

Synthesis and activity of 4,5-diarylimidazoles as human CB1 receptor inverse agonists

Structure-activity relationship studies directed toward the optimization of 4,5-diarylimidazole-2-carboxamide analogs as human CB1 receptor inverse agonists resulted in the discovery of the two amide derivatives 24a and b (hCB1 IC50 = 6.1 and 4