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Diethyl 6-oxo-n-heptylphosphonate is an organic compound with the chemical formula C11H21O3P. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 234.26 g/mol. diethyl 6-oxo-n-heptylphosphonate is a derivative of phosphonic acid, featuring a six-carbon chain with a carbonyl group at the sixth position and a phosphonate group attached to the terminal carbon. It is synthesized by reacting diethyl phosphite with 6-oxo-n-heptanal, and it is used as an intermediate in the production of various pharmaceuticals and agrochemicals. Due to its reactivity and potential applications, diethyl 6-oxo-n-heptylphosphonate is a significant compound in the field of organic chemistry.

1068-06-0

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1068-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1068-06-0 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 1068-06:
(6*1)+(5*0)+(4*6)+(3*8)+(2*0)+(1*6)=60
60 % 10 = 0
So 1068-06-0 is a valid CAS Registry Number.

1068-06-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 6-oxo-n-heptylphosphonate

1.2 Other means of identification

Product number -
Other names .(6-Oxo-heptyl)-phosphonsaeure-diaethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:1068-06-0 SDS

1068-06-0Downstream Products

1068-06-0Relevant 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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