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2-Chloroethyl 2,4-dichlorophenyl ethyl phosphate is a chemical compound with the molecular formula C10H10Cl3O4P. It is an organophosphate ester, which is a type of organophosphorus compound. 2-chloroethyl 2,4-dichlorophenyl ethyl phosphate is characterized by the presence of a phosphate group (PO4) attached to an ethyl group (C2H5), a 2-chloroethyl group (C2H4Cl), and a 2,4-dichlorophenyl group (C6H3Cl2). Organophosphate esters are known for their potential use as pesticides, flame retardants, and plasticizers. However, due to their toxicity and environmental concerns, their use is often regulated or restricted. The specific properties and applications of 2-chloroethyl 2,4-dichlorophenyl ethyl phosphate would depend on its chemical structure and reactivity, which can be influenced by the presence of the chloro and phosphate groups.

729-70-4

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729-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 729-70-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 729-70:
(5*7)+(4*2)+(3*9)+(2*7)+(1*0)=84
84 % 10 = 4
So 729-70-4 is a valid CAS Registry Number.

729-70-4Downstream Products

729-70-4Relevant 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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