1832-64-0

Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
Phosphonic acid, methyl-, mono(4-nitrophenyl) ester is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the development of novel compounds with potential therapeutic and pesticidal properties.
Used in Chelation Therapy:
Due to its strong metal-binding affinity, Phosphonic acid, methyl-, mono(4-nitrophenyl) ester is employed in chelation therapy. It can form stable complexes with metal ions, aiding in the treatment of heavy metal poisoning and facilitating the removal of toxic metals from the body.
Used as a Corrosion Inhibitor:
Phosphonic acid, methyl-, mono(4-nitrophenyl) ester is utilized as a corrosion inhibitor in various industrial applications. Its ability to form protective films on metal surfaces helps prevent corrosion and extends the service life of equipment and structures.
Used in the Production of Phosphonate-Based Polymers:
Phosphonic acid, methyl-, mono(4-nitrophenyl) ester is also used in the synthesis of phosphonate-based polymers, which exhibit unique properties such as self-healing, flame retardancy, and improved mechanical strength. These polymers have potential applications in various industries, including aerospace, automotive, and electronics.
Used in Chemical Research:
Phosphonic acid, methyl-, mono(4-nitrophenyl) ester serves as a valuable research tool in the field of chemistry. Its unique properties and reactivity make it an ideal candidate for studying various chemical reactions and mechanisms, contributing to the advancement of scientific knowledge.
However, it is crucial to handle Phosphonic acid, methyl-, mono(4-nitrophenyl) ester with care, as it is toxic and can cause skin and eye irritation upon contact. Proper safety measures, such as wearing protective gear and working in a well-ventilated area, should be taken to minimize potential health risks.

Upstream product

• 100-02-7 4-nitro-phenol 
• 1932-59-8 Methanphosphonsaeure-anhydrid 
• 6395-57-9 O,O-di-4-nitrophenyl methylphosphonate 
• 676-97-1 methylphosphonic acid dichloroanhydride 

Downstream Products

• 1428268-01-2 O-(2-fluoroethyl)-O-(p-nitrophenyl) methylphosphonate 
• 100-02-7 4-nitro-phenol 
• 498-00-0 4-hydroxymethyl-2-methoxyphenol 
• 1428268-16-9 C₁₆H₁₈NO₇PS₂ 
• 4230-69-7 C₁₀H₁₃BrNO₄PS 
• 4230-67-5 2-bromoethyl 4-nitrophenyl methyl(sulfanylidene)phosphonite 
• 889-14-5 O-2-fluoroethyl-O-p-nitrophenyl methyphosphonothionate 
• 1428268-08-9 2-[(4-methylbenzenesulfonyl)oxy]ethyl 4-nitrophenyl methanephosphonate 
• 1428268-07-8 2-iodoethyl 4-nitrophenyl methylphosphonate 
• 1428268-05-6 C₁₀H₁₃BrNO₅P 
• 1428268-03-4 2-bromo 4-nitrophenyl methylphosphonate 

Relevant academic research and scientific papers

The influence of hydrophobic amines on hydrolysis of bis(p-nitrophenyl) methylphosphonate in micellar solutions of cetylpyridinium bromide

The kinetics of hydrolysis of bis(p-nitrophenyl) methylphosphonate in the presence of primary aliphatic amines in aqueous micellar solutions of cetylpyridinium bromide was studied. The reaction proceeds via two routes, alkaline hydrolysis and amine-cataly

Balancing Specificity and Promiscuity in Enzyme Evolution: Multidimensional Activity Transitions in the Alkaline Phosphatase Superfamily

Highly proficient, promiscuous enzymes can be springboards for functional evolution, able to avoid loss of function during adaptation by their capacity to promote multiple reactions. We employ a systematic comparative study of structure, sequence, and sub

Synthesis and anti-acetylcholinesterase properties of novel β- And γ-substituted alkoxy organophosphonates

Activated organophosphate (OP) insecticides and chemical agents inhibit acetylcholinesterase (AChE) to form OP-AChE adducts. Whereas the structure of the OP correlates with the rate of inhibition, the structure of the OP-AChE adduct influences the rate at

CHOLINESTERASE INHIBITORS

The invention provides compounds that inhibit cholinesterases, such as acetylcholinesterase and butyrylcholinesterase. Such compounds are useful to prevent or treat exposure of a patient (e.g., a human) to an organophosphoric nerve agent (e.g., sarin and

Catalysis of the hydrolysis of esters of phosphorus acids by n-decylammonium chloride/n-decylamine mixed micelles

The effect of n-decylammonium chloride/n-decylamine mixed micelles on the rate of hydrolysis of aryl esters of acids of four-coordinate phosphorus was studied spectrophotometrically. The shape of the concentration curves is characteristic of the micellar