110719-01-2

Basic information

• Product Name: 1-Heptanone, 7-iodo-1-phenyl-
• Synonyms: 1-Heptanone,7-iodo-1-phenyl
• CAS NO: 110719-01-2
• Molecular Formula: C13H17IO
• Molecular Weight: 316.182
• Mol File: 110719-01-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 359.3±25.0 °C(Predicted)
• Density: 1.422±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-Heptanone, 7-iodo-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Heptanone, 7-iodo-1-phenyl-(110719-01-2)
• EPA Substance Registry System: 1-Heptanone, 7-iodo-1-phenyl-(110719-01-2)

Safety Data

• Hazardous Substances Data: 110719-01-2(Hazardous Substances Data)

Upstream product

• 37908-41-1 1-hydroperoxy-1-phenylcycloheptane 
• 502-42-1 cycloheptanone 
• 17257-32-8 1-propylcycloheptanol 
• 2082-21-5 1-phenylcycloheptanol 

Downstream Products

• 113274-37-6 C₆H₅C(O)(CH₂)6ZnI 
• 227018-70-4 (E)-7-iodo-1-phenyl-2-hepten-1-one 

Relevant articles and documents

Far-end halogenated alkyl ketone taking HX as halogen source and synthesis method of far-end halogenated alkyl ketone

The invention relates to a far-end halogenated alkyl ketone taking HX as a halogen source and a synthesis method of the far-end halogenated alkyl ketone. The method comprises the following steps that: cycloalkyl peroxy alcohol and a copper acetate catalyst are added in a nitrogen atmosphere, then HCl, HBr and an HI solution are added as halogens, and stirring is carried out at normal temperature; after a reaction is finished, sufficient water is added to extract a reaction solvent N-methyl pyrrolidone, performing washing with saturated saline solution, an organic phase is dried with anhydrous sodium sulfate, the organic phase is concentrated under reduced pressure, so that the solvent can be removed; and column chromatography is performed on the organic phase to obtain a target product. According to the far-end halogenated alkyl ketone taking the HX as the halogen source and the synthesis method of the far-end halogenated alkyl ketoneinvention, industrial bulk raw materials HCl, HBr and an HI solution are used as the halogen source, free radical halogenation of C-C bond cracking is realized, and the far-end halogenated alkyl alkyl ketone compound is obtained with high yield; the byproduct of the reaction is water, so that the environmental pollution is reduced, and the industrial production benefit is greatly improved.

In-situ-generation of alkylsilyl peroxides from alkyl hydroperoxides and their subsequent copper-catalyzed functionalization with organosilicon compounds

Alkylsilyl peroxides were generated in situ from the corresponding alkyl hydroperoxides using organosilicon compounds of the type Me3SiX (X = CN, N3, and halogens) and an amine base. Subsequent in situ copper-catalyzed homolytic cleavage of the alkylsilyl peroxides afforded alkyl radicals, which were then trapped with X (X = CN, N3, and halogens) to furnish products with new carbon-carbon, carbon-nitrogen, or carbon-halogen bonds in good to high yields.

Visible-light-enhanced ring opening of cycloalkanols enabled by br?nsted base-tethered acyloxy radical induced hydrogen atom transfer-electron transfer

A metal-free ring opening/halogenation of cycloalkanols, which combines both PPO/TBAX oxidant system and blue LEDs irradiation, is presented. This method produces diverse γ, α, and even more remotely halogenated ketones in moderate to excellent yields under mild conditions. Interestingly, experimental and computational studies demonstrate the novel ring size-dependent concerted/stepwise (four-/five- to eight-membered rings) hydrogen atom transfer-electron transfer induced by Br?nsted base-tethered acyloxy radical, which indicates distinct advantages brought by the cyclic structure of diacyl peroxides.