20061-84-1

Usage

Uses

Used in Agricultural and Horticultural Industries:
DIETHYL CYCLOHEXYLAMINOVINYL PHOSPHATE is used as an insecticide and acaricide for controlling a variety of pests in these industries. Its application is aimed at protecting crops from damage caused by insects and mites, thereby ensuring higher yields and quality produce.
Used as a Chemical Intermediate:
In the chemical industry, DIETHYL CYCLOHEXYLAMINOVINYL PHOSPHATE is utilized as an intermediate in the production of other chemicals. Its role in chemical synthesis contributes to the creation of a range of products that may have various applications in different sectors.
Safety Precautions:
Given its toxic nature, DIETHYL CYCLOHEXYLAMINOVINYL PHOSPHATE requires careful handling to prevent harm to humans and non-target organisms. It is crucial to adhere to all safety guidelines and regulations when using this chemical to minimize potential risks to human health and the environment.

InChI:InChI=1/C12H24NO3P/c1-3-15-17(14,16-4-2)11-10-13-12-8-6-5-7-9-12/h10-13H,3-9H2,1-2H3/b11-10+

Upstream product

• 1606-75-3 (2-oxoethyl)phosphonic acid diethyl ester 
• 108-91-8 cyclohexylamine 
• 7598-61-0 diethyl phosphonoacetaldehyde diethyl acetal 

Downstream Products

• 19897-11-1 seq.trans-3-Formylmethylen-17β-benzoyloxy-5α-androstan 
• 23594-02-7 3,3-bis(4-chlorophenyl)acrylaldehyde 
• 5392-40-5 (E/Z)-3,7-dimethyl-2,6-octadienal 
• 1713-63-9 cyclohexylideneacetaldehyde 

Relevant academic research and scientific papers

Synthesis and biological evaluation of cycloalkylidene carboxylic acids as novel effectors of Ras/Raf interaction

The protooncogenes Ras and Raf play important roles in signal transduction pathways regulated by mitogen-activated protein kinases. Mutations of Ras that arrest the protein in its active state are frequently implicated in tumor formation. We used Ras and Raf proteins in the yeast two-hybrid system to search for natural or synthesized substances capable of modulating Ras/Raf interaction by specifically binding to one of the interacting partners. We found that cycloalkylidene carboxylic acids enhanced Ras/Raf interaction by acting on the cysteine-rich domain of Raf. Several analogues of the active substance 2-cyclohexylidene propanoic acid were synthesized and the importance of the semicyclic double bond in the stabilization of Ras/Raf interaction was demonstrated. Variation of the size and the substituents of the cyclic system as well as the length of the carboxylic acid resulted in enhanced Ras/Raf interaction.

A New Entry to the C12H12 Energy Surface: Pyrolysis and Photolysis of trans-β-nona-2,4,6-trienyl>acrolein Tosylhydrazone Saltz

Thermal decomposition of the lithium salt of trans-β-nona-2,4,6-trienyl>acrolein tosylhydrazone (8) results in the formation of pentacyclo2,12.03,7.04,11>dodeca-5,9-diene (12), exo- and endo-tricyclo2,5>dodeca-3,7,9,11-tetraenes (9 and 10), 1,2-benzocycloocta-1,3,7-triene (11), and syn- and anti-9-(5-pyrazolyl)bicyclonona-2,4,7-trienes (14 and 13).The low-temperature photolysis of the sodium salt of tosylhydrazone 8 gives anti-9-(2-cyclopropen-1-yl)bicyclonona-2,4,6-triene (20), which affords pentacyclo2,4.03,10.05,9>dodeca-6-11-diene (22) on thermolysis.Hydrocarbon 12 was formed in the photolysis of the sodium salt of trans-β-nona-2,4,7-trienyl>acrolein tosylhydrazone (15; available by thermal rearrangement of tosylhydrazone 8) as the sole C12H12 product.Structure determinations and mechanistic investigations are discussed.