54376-65-7 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Diethylaminobenzaldehyde oxime is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Dye and Pigment Production:
As an important intermediate, 4-Diethylaminobenzaldehyde oxime is utilized in the production of dyes and pigments, enhancing the color properties and stability of these compounds in different applications.
Used in Chemical and Industrial Applications:
4-Diethylaminobenzaldehyde oxime is employed as a chelating agent, forming coordination complexes with metal ions, which is beneficial in various chemical processes and industrial applications.
Used in Polymer Additive Preparation:
4-DIETHYLAMINOBENZALDEHYDE OXIME is used as a precursor in the preparation of polymer additives, improving the performance and properties of polymers in diverse applications.
Used in Surfactant and Corrosion Inhibitor Production:
4-Diethylaminobenzaldehyde oxime is utilized in the production of surfactants and corrosion inhibitors, enhancing the performance of these products in various industrial processes.
Used in Catalyst and Antioxidant Applications:
Due to its catalytic and antioxidant properties, 4-Diethylaminobenzaldehyde oxime is employed in applications requiring enhanced reaction rates and protection against oxidative degradation.
Check Digit Verification of cas no
The CAS Registry Mumber 54376-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,7 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54376-65:
(7*5)+(6*4)+(5*3)+(4*7)+(3*6)+(2*6)+(1*5)=137
137 % 10 = 7
So 54376-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O/c1-3-13(4-2)11-7-5-10(6-8-11)9-12-14/h5-9,14H,3-4H2,1-2H3/b12-9+
54376-65-7Relevant academic research and scientific papers
Effect of the Steric Hindrance and Branched Substituents on Visible Phenylamine Oxime Ester Photoinitiators: Photopolymerization Kinetics Investigation through Photo-DSC Experiments
Chen, Ching-Chin,Chen, Yung-Chung,Graff, Bernadette,Hammoud, Fatima,Hijazi, Akram,Huang, Tung-Liang,Lalevée, Jacques,Lee, Zhong-Han
, (2021/11/04)
In this work, free radical photopolymerization (FRP) kinetics for series of different phenylamine oxime ester structures (DMA–P, DEA–P, DMA–M, TP–2P, TP–2M and TP–3M) was investigated. Steric hindrance and branched substituents were prepared to realize th
Synthesis and in vitro evaluation of neutral aryloximes as reactivators of Electrophorus eel acetylcholinesterase inhibited by NEMP, a VX surrogate
Cavalcante, Samir F. de A.,Kitagawa, Daniel A.S.,Rodrigues, Rafael B.,Bernardo, Leandro B.,da Silva, Thiago N.,dos Santos, Wellington V.,Correa, Ana Beatriz de A.,de Almeida, Joyce S.F.D.,Fran?a, Tanos C.C.,Ku?a, Kamil,Simas, Alessandro B.C.
, (2019/06/24)
Casualties caused by nerve agents, potent acetylcholinesterase inhibitors, have attracted attention from media recently. Poisoning with these chemicals may be fatal if not correctly addressed. Therefore, research on novel antidotes is clearly warranted. Pyridinium oximes are the only clinically available compounds, but poor penetration into the blood-brain barrier hampers efficient enzyme reactivation at the central nervous system. In searching for structural factors that may be explored in SAR studies, we synthesized and evaluated neutral aryloximes as reactivators for acetylcholinesterase inhibited by NEMP, a VX surrogate. Although few tested compounds reached comparable reactivation results with clinical standards, they may be considered as leads for further optimization.
