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Phosphoric acid ethyl ester-(2-chloro-ethyl ester)-phenyl ester is a complex organic compound with the chemical formula C10H13Cl2O5P. It is a derivative of phosphoric acid, featuring an ethyl group, a 2-chloro-ethyl group, and a phenyl group esterified to the phosphoric acid backbone. phosphoric acid ethyl ester-(2-chloro-ethyl ester)-phenyl ester is characterized by its potential reactivity due to the presence of the chlorine atoms, which can participate in various chemical reactions, such as nucleophilic substitutions. It is an example of a phosphoric acid triester, where three ester groups are attached to the central phosphorus atom. Such compounds are of interest in organic chemistry and may have applications in the synthesis of pharmaceuticals or as intermediates in chemical processes.

6719-90-0

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6719-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6719-90-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6719-90:
(6*6)+(5*7)+(4*1)+(3*9)+(2*9)+(1*0)=120
120 % 10 = 0
So 6719-90-0 is a valid CAS Registry Number.

6719-90-0Downstream Products

6719-90-0Relevant academic research and scientific papers

Synthesis, fungitoxicity and quantitative structure activity relationship of O-aryl O-2-chloroethyl O-ethyl phosphates

Singh, Neera

, p. 257 - 261 (2007/10/03)

Nineteen new O-aryl O-2-chloroethyI O-ethyl phosphates 3 have been synthesised and tested for their fungicidal activity in vitro against Rhizoctonia bataticola and Alternaria alternate. O-2-Chloroethyl O-ethyl O- (pentachlorophenyl) phosphate 3s shows highest activity against both the tested fungi and possesses better activity compared to the standard ediphenphos. Quantitative structure activity relationship studies provide excellent correlation between fungicidal activities and physico-chemical parameters like hydrophobicity (Σπ), electronic effect (Σσ) and few position specific STERIMOL parameters like ΣL(o), ΣL(m), ΣB1(o) and Σ4(m) of phenyl ring substituents.

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