2817-45-0

Usage

Uses

Used in Chemical Reactions:
Phosphoramidic acid is used as a reactive compound for [application reason] due to its significant reactivity towards hydroxyl groups, allowing it to participate in various chemical reactions.
Used in Synthesis Processes:
In the chemical industry, phosphoramidic acid is used as an intermediate or building block for [application reason] in the synthesis of more complex molecules or compounds, taking advantage of its reactivity.
Used in Research and Development:
Phosphoramidic acid is utilized as a research compound for [application reason] in academic and industrial laboratories to explore its properties, reactivity, and potential applications in new chemical processes or products.

InChI:InChI=1/H4NO3P/c1-5(2,3)4/h(H4,1,2,3,4)

Upstream product

• 7732-18-5 water 
• 2015-56-7 diphenylphosphoroamidate 
• 10043-91-1 diamidophosphoric acid 
• 7782-77-6 cis-nitrous acid 
• 7664-41-7 ammonia 
• 814-49-3 diethyl chlorophosphate 
• 18027-03-7 Dichlorphosphorsaeure-trimethylsilylamid 
• 13823-49-9 potassium monophosphoramidate 
• 7601-90-3 perchloric acid 
• 100576-20-3 P₆N₆O₁₂H₁₂ 
• 7783-06-4 hydrogen sulfide 
• 1310-73-2 sodium hydroxide 

Downstream Products

• 7722-76-1 ammonium dihydrogen phosphate 
• 12436-32-7 H₅P₃O₉ 
• 727355-49-9 H₆P₄O₁₀ 
• 7647-01-0 hydrogenchloride 
• 13966-08-0 dichlorophosphinylphosphorimidic trichloride 
• 10025-87-3 trichlorophosphate 
• 41744-81-4 H₃NO₃P^(1-) 

Relevant academic research and scientific papers

Phosphonamide ACAT inhibitors

The present invention is directed to compounds useful for the regulation of cholesterol of Formula I, methods for using them and pharmaceutical compositions thereof, STR1 wherein Ar and Ar1 are each independently selected from unsubstituted or substituted phenyl which substituents are from 1-5 in number and are each independently selected from alkyl, alkoxy, hydroxy, halogen, nitro, trifluoromethyl, COOH, and COOalkyl; X is --NH--, --O--, --S--, or --(CH2)0-4 --, and R is hydrogen, alkyl, or phenyl.

Solubilized imidazole pro-drugs

The N-phosphorylation of basic nitrogenous drug compounds to produce pro-drugs with enhanced water solubility or lipid solubility, or reduced toxicity, is disclosed. Drugs containing amine, amidine, quanidine, isourea, isothiourea and biguanide functions may be converted to such pro-drugs. The pro-drugs are hydrolyzed in the body, regenerating the original drugs with the release of a salt of phosphoric acid.

Acylation products of bis(2-imidazolin-2-ylhydrazones) of 9,10-anthracenedicarboxaldehyde

N-acylated derivatives of bis(2-imidazolin-2-ylhydrazones) of 9,10-anthracenedicarboxaldehyde, useful as anti-cancer agents against certain strains in mice, are disclosed and described, including processes for manufacture and use.