33862-44-1

Usage

InChI:InChI=1/C12H13N2O3P/c13-14-18(15,16-11-7-3-1-4-8-11)17-12-9-5-2-6-10-12/h1-10H,13H2,(H,14,15)

Upstream product

• 2524-64-3 chlorophosphoric acid diphenyl ester 

Downstream Products

• 79579-40-1 benzylidene-hydrazidophosphoric acid diphenyl ester 
• 33858-85-4 N'-isopropylidene-hydrazidophosphoric acid diphenyl ester 
• 16001-00-6 μ-hydrazido-diphosphoric acid tetraphenyl ester 
• 33858-81-0 N'-[1-Phenyl-eth-(E)-ylidene]-phosphorohydrazidic acid diphenyl ester 
• 17938-43-1 N-Trimethylsilyl-hydrazidophosphorsaeure-diphenylester 
• 135419-55-5 2-[(Diphenoxy-phosphoryl)-hydrazono]-cyclopentanecarboxylic acid benzyl ester 
• 135419-52-2 2-[(Diphenoxy-phosphoryl)-hydrazono]-cyclopentanecarboxylic acid ethyl ester 
• 125313-00-0 N'-[1-Phenyl-meth-(E)-ylidene]-phosphorohydrazidic acid diphenyl ester 
• 125313-09-9 N'-[(E)-1,3-Diphenyl-prop-2-en-(Z)-ylidene]-phosphorohydrazidic acid diphenyl ester 
• 130307-54-9 diacetyl mono(diphenylphosphonyl)hydrazone 
• 130307-59-4 N'-[2-[(Diphenoxy-phosphoryl)-hydrazono]-1-methyl-prop-(E)-ylidene]-phosphorohydrazidic acid diphenyl ester 
• 125313-05-5 N'-[1-Phenyl-eth-(E)-ylidene]-phosphorohydrazidic acid diphenyl ester 
• 125313-08-8 N'-[(E)-1-Methyl-3-phenyl-prop-2-en-(E)-ylidene]-phosphorohydrazidic acid diphenyl ester 
• 40970-52-3 C₂₀H₂₀N₃O₃PS 

Relevant academic research and scientific papers

Quinazolone thiazole compounds, and preparation method and application thereof

The invention relates to quinazolone thiazole compounds, and a preparation method and an application thereof, and belongs to the technical field of chemical synthesis. The quinazolone thiazole compounds are represented by general formula I to IV. The compounds have a certain inhibitory activity to one or more of Gram-positive bacteria, Gram-negative bacteria and fungi, and can be used to prepare antibacterial and/or antifungal drugs in order to provide efficient and safe drug candidate drugs for clinical ant-microbial treatment and contribute to solve clinical treatment problems such as increasing drug resistance, stubborn pathogenic microorganisms and emerging harmful microorganisms.

Phosphorhydrazides as urease and acetylcholinesterase inhibitors: biological evaluation and QSAR study

New phosphorhydrazide compounds (1–7, 13, 15–16) and thiophosphorhydrazide (14 and 17) were synthesized and characterized by 31P, 13C, 1H NMR and IR spectroscopy. Furthermore, the crystal structure of compound (C6/su