2175-86-2

Usage

Uses

Used in Pharmaceutical Industry:
(4-NITRO-PHENYL)-PHOSPHONIC ACID is used as a chemical intermediate for the synthesis of pharmaceutical compounds. Its unique structure allows it to be a building block for creating new drugs with potential therapeutic applications.
Used in Agricultural Industry:
In the agricultural sector, (4-NITRO-PHENYL)-PHOSPHONIC ACID is utilized as a reagent in chemical reactions to produce agrochemicals. Its role in the synthesis of various compounds makes it a valuable asset in developing new pesticides or other agricultural products.
Used as a Reagent in Chemical Reactions:
(4-NITRO-PHENYL)-PHOSPHONIC ACID is employed as a reagent in various chemical reactions, facilitating the synthesis of a wide range of organic compounds for different applications across various industries.
Safety Precautions:
It is crucial to handle (4-NITRO-PHENYL)-PHOSPHONIC ACID with care, as it may pose risks if ingested or comes into contact with the skin or eyes. Proper safety measures should be taken to minimize potential harm during its use and manipulation.

InChI:InChI=1/C6H6NO5P/c8-7(9)5-1-3-6(4-2-5)13(10,11)12/h1-4H,(H2,10,11,12)

Upstream product

• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 100-01-6 4-nitro-aniline 
• 54211-72-2 C₂₄H₂₄N₃O₇P 

Downstream Products

• 339-46-8 (4-nitro-phenyl)-phosphonic acid mono-(2,2,2-trifluoro-ethyl ester) 
• 34909-18-7 4-(Nitrophenyl)phosphonsaeure-dichlorid 
• 5337-17-7 4-aminophenylphosphonic acid 
• 172954-49-3 (1R,2R,3S,5S)-3-[Hydroxy-(4-nitro-phenyl)-phosphinoyloxy]-8-methyl-8-aza-bicyclo[3.2.1]octane-2-carboxylic acid methyl ester 
• 100926-20-3 C₁₃H₁₃N₂O₄P 
• 100120-39-6 (4-amino-phenyl)-phosphonic acid methyl ester-[2]pyridylamide 
• 100616-87-3 (4-amino-phenyl)-phosphonic acid ethyl ester-[2]pyridylamide 
• 104440-24-6 (4-amino-phenyl)-phosphonic acid ethyl ester-pyrimidin-2-ylamide 
• 100517-59-7 (4-nitro-phenyl)-phosphonic acid methyl ester-[2]pyridylamide 
• 100796-47-2 (4-nitro-phenyl)-phosphonic acid ethyl ester-[2]pyridylamide 
• 100882-13-1 (4-nitro-phenyl)-phosphonic acid ethyl ester-(5-methyl-[2]pyridylamide) 
• 98334-24-8 (4-amino-phenyl)-phosphonic acid monomethyl ester 
• 98489-27-1 (4-amino-phenyl)-phosphonic acid monoethyl ester 
• 7477-55-6 (4-amino-phenyl)-phosphonic acid ethyl ester-benzylamide 

Relevant academic research and scientific papers

ETUDE D'UN SCHEMA DE SYNTHESE PEPTIDIQUE INTRAMOLECULAIRE A L'AIDE DE DERIVES DU PHOSPHORE TETRAEDRIQUE

A new scheme of repetitive and controlled peptide synthesis offers two advantages compared to the usual methods of synthesis: two steps only are used for the prolongation of a peptide chain with an amino-acid residue and the risk of racemisation is minimized.The two postulated steps are verified particularly by the rearrangement, in an alkaline alcoholic medium, of phosphordiamides 1 incorporating one amino-acid residue, leading to the formation of the peptide derivatives 6 and 8.The severe limitations of this method are discussed.

Phosphorus-fluorine chemistry. XIII. The adduct of nitrosyl fluoride with phenyltetrafluorophosphorane. New fluorophosphates

Nitrosyl fluoride was found to react with phenyltetrafluorophosphorane to form a solid, thermally unstable 1:1 adduct. Evidence for the formulation of this adduct as a nitrosyl salt, NO+C6H5PF5-, based on various chemical reactions, is presented. The novel fluoroanions, R(Ar)PF5-, together with alkyl(aryl)dialkylaminotrifluorophosphoranes, R(Ar)PF3NR2, are also obtained in the form of stable dialkylammonium salts upon dialkylaminolysis of tetrafluorophosphoranes, R(Ar)PF4. The stereochemistry of the R(Ar)PF5- anions, and of the alkyl(aryl)dialkylaminotrifluorophosphoranes, based on n.m.r. spectroscopic studies, is discussed. In contrast to nitrosyl fluoride, nitryl fluoride reacted with phenyltetrafluorophosphorane with direct nitration of the aromatic ring.