109467-74-5

Usage

Uses

Used in Plastics and Polymers Industry:
Phosphoric acid, 1-cyclohexen-1-yl diphenyl ester is used as a plasticizer for enhancing the flexibility, durability, and tensile strength of plastic and rubber materials. It is particularly utilized in the manufacturing of flexible PVC products such as cables, flooring, and tubing, as well as in the production of synthetic rubbers.
Precautions:
Exposure to Phosphoric acid, 1-cyclohexen-1-yl diphenyl ester can be harmful, causing irritation to the skin, eyes, and respiratory system. In high concentrations, it can be toxic if ingested or inhaled. Therefore, proper handling and protective measures are necessary when working with this chemical compound.

Upstream product

• 108-94-1 cyclohexanone 
• 2524-64-3 chlorophosphoric acid diphenyl ester 

Downstream Products

• 108803-39-0 (2-Hydroxy-phenyl)-phosphonic acid cyclohex-1-enyl ester phenyl ester 
• 108803-39-0 (1-cyclohexenyl)bis(2-hydroxyphenyl)phosphinate 
• 1546-11-8 4'-fluoro-2,3,4,5-tetrahydro-1,1'-biphenyl 
• 225935-96-6 3-(cyclohexen-1-yl)aniline 
• 54607-03-3 2-(cyclohex-1-en-1-yl)naphthalene 
• 20758-60-5 1-(4-methoxyphenyl)cyclohexene 
• 40358-51-8 1-cyclohex-1-enyl-naphthalene 
• 22618-48-0 1-(cyclohexen-1-yl)-2-methoxybenzene 
• 771-98-2 1-Phenylcyclohexene 
• 3282-53-9 1-butyl-1-cyclohexene 
• 15232-87-8 1-octylcyclohex-1-ene 
• 22618-51-5 2'-methyl-2,3,4,5-tetrahydro-1,1'-biphenyl 
• 23386-15-4 2-(cyclohex-1-en-1-yl)benzo[d]oxazole 
• 66730-34-5 2-(cyclohex-1-en-1-yl)benzo[d]thiazole 

Relevant academic research and scientific papers

Palladium-catalyzed cross coupling of Grignard reagents with in situ-derived enol phosphates

A useful, one-pot protocol has been developed for the conversion of enolizable ketones to alkylated or arylated olefins by Pd-catalyzed cross coupling of in situ-generated enol phosphate intermediates with Grignard reagents.

Process for preparing vinylaromatic compounds

The present invention provides a process for preparing a vinylaromatic compound comprising reacting an arylmetal reagent selected from arylmagnesium reagents and aryllithium reagents with a vinylphosphate in the presence of a palladium catalyst. The present invention also provides a process for preparing a vinylphosphate comprising reacting an enolizable ketone with a sterically hindered Grignard reagent and a halophosphate diester.

Nickel-catalyzed cross-couplings of cyclohexenyl phosphate and arylboronic acids

The Nickel-catalyzed cross-coupling reaction of cyclohexenylphosphate with a variety of arylboronic acids is described here for the first time. This methodology opens the door to other palladium or nickel-catalyzed coupling reactions involving vinyl phosphates.

Synthesis of β-Keto Phosphonates from Vinyl Phosphates via a 1,3-Phosphorus Migration

A new method for the preparation of β-keto phosphonates has been developed, involving rearrangement of vinyl phosphates upon treatment with strong base.Because this approach ultimately relies upon electrophilic dialkyl phosphorochloridates as the phosphor