4964-49-2 Usage
Description
1-(2-Aminophenyl)ethan-1-one oxime, also known as APB-OH, is a chemical compound with the molecular formula C8H9NO. It is an oxime derivative of 1-(2-aminophenyl)ethan-1-one and is commonly used in organic synthesis and pharmaceutical research. APB-OH is a white crystalline solid that serves as a reagent in the preparation of various organic compounds and as a building block in the synthesis of pharmaceutical drugs and other biologically active compounds. It has also been investigated for its potential use in the development of new drugs and therapies for various medical conditions, making it an important compound in the field of organic chemistry and drug discovery.
Uses
Used in Organic Synthesis:
1-(2-Aminophenyl)ethan-1-one oxime is used as a reagent for the preparation of various organic compounds. Its unique structure allows for versatile reactions and the formation of a wide range of products, making it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-Aminophenyl)ethan-1-one oxime is used as a building block in the synthesis of pharmaceutical drugs and other biologically active compounds. Its structural properties enable the development of new drug candidates with potential therapeutic applications.
Used in Drug Discovery:
1-(2-Aminophenyl)ethan-1-one oxime has been investigated for its potential use in the development of new drugs and therapies for various medical conditions. Its unique chemical properties and reactivity make it a promising candidate for the creation of novel therapeutic agents.
Overall, 1-(2-Aminophenyl)ethan-1-one oxime is a versatile and important compound in the fields of organic chemistry, pharmaceutical research, and drug discovery, with applications in the synthesis of organic compounds, development of pharmaceutical drugs, and exploration of new therapeutic agents for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 4964-49-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4964-49:
(6*4)+(5*9)+(4*6)+(3*4)+(2*4)+(1*9)=122
122 % 10 = 2
So 4964-49-2 is a valid CAS Registry Number.
4964-49-2Relevant articles and documents
Preparation, characterization and biological activity of new tridentate imine-oxime ligand (H2L) and Its metal complexes
Al-Zaidi, Basim H.,Ismail, Ahmed H.,Naseaf, Ali N.,Khamis, Wessal
, p. 1157 - 1164 (2018)
The new tridentate Schiff-oxime ligand 1-[2-(2,4-dihydroxybenzylidene)aminophenyl]ethanone oxime (H2L), prepared via condensation of equal amounts of 1-(2-aminophenyl)ethanone oxime and 4-hydroxysalicylaldehyde. H2L ligand characterized by using FTIR, UV-
A convenient approach to 2,4-disubstituted quinazoline-3-oxides using active MnO2 as the oxidant
Ye, Xinglin,Chen, Zhiyuan,Zhang, Zhipeng,Fu, Yang,Deng, Zhihong,Peng, Yiyuan
supporting information, p. 682 - 689 (2019/09/06)
Using cheap, readily available, and economic active MnO2 as an oxidant, a series of 2,4-disubstituted quinazoline-3-oxides were synthesized in good to excellent yields by oxidation of the corresponding 1,2-dihydroquinazoline-3-oxides under mild
Visible light-mediated synthesis of quinazolines from 1,2- dihydroquinazoline 3-oxides
Chen, Yi-Chou,Yang, Ding-Yah
, p. 10438 - 10444 (2013/11/19)
A series of quinazolines were synthesized in good to excellent yields by exposing 1,2-dihydroquinazoline 3-oxides to visible light in acetonitrile without the presence of any external sensitizers. The only exception was the 2-(p-nitrophenyl)-substituted s
