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Diethyl 5-oxo-n-hexylphosphonate is an organic compound with the chemical formula C10H19O3P. It is a colorless liquid at room temperature and is soluble in organic solvents. diethyl 5-oxo-n-hexylphosphonate is a derivative of phosphonic acid, featuring a five-carbon chain with a ketone group at the fifth carbon and a phosphonate group attached to the terminal carbon. It is synthesized through the reaction of diethyl phosphite with 5-oxohexanal, and it is used as an intermediate in the production of various organophosphorus compounds, such as flame retardants, pesticides, and pharmaceuticals. Due to its reactivity and potential applications, diethyl 5-oxo-n-hexylphosphonate is a significant chemical in the field of organic chemistry and material science.

1068-04-8

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1068-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1068-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1068-04:
(6*1)+(5*0)+(4*6)+(3*8)+(2*0)+(1*4)=58
58 % 10 = 8
So 1068-04-8 is a valid CAS Registry Number.

1068-04-8Downstream Products

1068-04-8Relevant academic research and scientific papers

A new, effective approach for the C-C bond formation utilizing 1-, 2- and 3-phosphonyl substituted radicals derived from iodoalkylphosphonates and n-Bu3SnH/Et3B/O2 system

Balczewski,Pietrzykowski

, p. 7291 - 7304 (2007/10/03)

A new, practical synthesis of highly substituted phosphonates utilizing 1-, 2- and 3-phosphonyl substituted radicals derived from iodoalkylphosphonates and a catalytic or stoichiometric amounts of the n-Bu3SnH/Et3B/O2 reagent is described.

A free radical approach to functionalization of phosphonates utilizing novel 2- and 3-phosphonyl radicals

Balczewski, Piotr,Pietrzykowski, Witold M.

, p. 13681 - 13694 (2007/10/03)

A general method for the phosphonyl C2-C3-C bond formation under the free radical, reductive conditions is described. The new approach is based on the synthesis of novel 2- and 3-phosphonyl radicals 6, 9 derived from the corresponding 2- and 3-halo (X = Cl, Br, I) substituted phosphonates 7, 10 and their reaction with alkenes 4. Functionalized phosphonates 5, 8 possessing the 2+2 and 3+2 elongated carbon chain were obtained in 24-73% yields.

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