111729-78-3

Basic information

• Product Name: Cyclohexanone, 2-[(4-bromophenyl)methylene]-, (E)-
• CAS NO: 111729-78-3
• Molecular Formula: C13H13BrO
• Molecular Weight: 265.15
• Mol File: 111729-78-3.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-[(4-bromophenyl)methylene]-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-[(4-bromophenyl)methylene]-, (E)-(111729-78-3)
• EPA Substance Registry System: Cyclohexanone, 2-[(4-bromophenyl)methylene]-, (E)-(111729-78-3)

Safety Data

• Hazardous Substances Data: 111729-78-3(Hazardous Substances Data)

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 6651-36-1 1-(Trimethylsilyloxy)cyclohexene 
• 119752-02-2 2-(hydroxy-(4-bromophenyl)methyl)cyclohexan-1-one 
• 108-94-1 cyclohexanone 
• 22780-11-6 1-(2,2,2-trichloroacetoxy)cyclohexene 

Downstream Products

• 1604009-91-7 C₁₆H₂₀O₃ 
• 133908-75-5 (+)-(2S)-2-<4-(2-Oxocyclohexylidenemethyl)phenyl>propionic acid 
• 133963-62-9 (-)-(2R)-2-<4-(2-Oxocyclohexylidenemethyl)phenyl>propionic acid 
• 1604009-87-1 C₁₆H₁₆O₃ 
• 1604010-95-8 C₁₅H₁₇BrO₂ 
• 139938-34-4 trans-N-benzyl-4-(4-bromophenyl)-4a,5,6,7-tetrahydro-4H-3,1-benzothiazine-2(1H)-thione 
• 139938-24-2 2-(α-(N-benzyl-thiocarbamoylthio)-4-bromobenzyl)-cyclohexan-1-one 

Relevant articles and documents

Selective synthesis of α,β-unsaturated ketones by dibutyltin dimethoxide-catalyzed condensation of aldehydes with alkenyl trichloroacetates

(Chemical Equation Presented) Various α,β-unsaturated ketones were stereoselectively synthesized in high yields up to 94% by a condensation reaction between alkenyl trichloroacetates and aldehydes using dibutyltin dimethoxide as a catalyst in the presence of methanol. This process is superior to the classical Claisen-Schmidt condensation with respect to mildness of the base catalyst and product selectivity.

Redox-Neutral Cobalt(III)-Catalyzed C-H Activation/Annulation of α,β-Unsaturated Oxime Ether with Alkyne: One-Step Access to Multisubstituted Pyridine

A redox neutral Co(III)-catalyzed annulation of α,β-unsaturated oxime ether with alkyne has been reported. Multisubstituted pyridines were synthesized in good yields without the use of any heavy metal oxidants. The developed methodology tolerates a variety of functional groups. Notably, this transformation has been applied to the late-stage modification of the bioactive molecule dehydropregnenolone.

Synthesis of 1H-isochromenes, 4H-chromenes, and ortho-aminocarbonitrile tetrahydronaphthalenes from the same reactants by using metal-free catalyst

A facile and rapid multicomponent synthesis of pharmaceutically diverse 1H-isochromenes, 4H-chromenes, and ortho-aminocarbonitrile tetrahydronaphthalenes has been developed from benzaldehyde, malononitrile, and cyclohexanone. Three different methods from the same reactants, solvent, temperature, and catalyst lead to three products with excellent yields. All the reactions were followed with the Michael addition and cyclization. In this study, morpholine was used as an active metal-free base catalyst that increases the yields of products and decreases the time of reactions.