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Ethyl phenyl (4-nitrophenyl)phosphonate is an organic compound with the chemical formula C14H14NO5P. It is a phosphonate ester derived from ethyl phenylphosphonate and 4-nitrophenol. ethyl phenyl (4-nitrophenyl)phosphonate is characterized by the presence of a phosphorus atom bonded to an ethyl group, a phenyl group, and a 4-nitrophenyl group. The 4-nitrophenyl group contains a nitro functional group attached to the para position of the phenyl ring, which imparts distinct chemical properties. Ethyl phenyl (4-nitrophenyl)phosphonate is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals, due to its ability to form stable derivatives and its potential reactivity in chemical transformations.

1776-93-8

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1776-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1776-93-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1776-93:
(6*1)+(5*7)+(4*7)+(3*6)+(2*9)+(1*3)=108
108 % 10 = 8
So 1776-93-8 is a valid CAS Registry Number.

1776-93-8Downstream Products

1776-93-8Relevant academic research and scientific papers

Direct Aryloxylation/Alkyloxylation of Dialkyl Phosphonates for the Synthesis of Mixed Phosphonates

Huang, Hai,Denne, Johanna,Yang, Chou-Hsun,Wang, Haobin,Kang, Jun Yong

, p. 6624 - 6628 (2018/05/14)

A strategy for the direct functionalization strategy of inertial dialkyl phosphonates with hydroxy compounds to afford diverse mixed phosphonates with good yields and functional-group tolerance has been developed. Mechanistic investigations involving both NMR studies and DFT studies suggest that an unprecedented highly reactive PV species (phosphoryl pyridin-1-ium salt), a key intermediate for this new synthetic transformation, is generated in situ from dialkyl phosphonate in the presence of Tf2O/pyridine.

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