1174046-74-2 Usage
Description
(3-Chloro-2-(diphenylmethyleneamino)pyridin-4(1H)-one is a chemical compound with the molecular formula C18H13ClN2O. It is an organic compound that contains a pyridine ring, a chlorine atom, and a diphenylmethyleneamino group. (3-Chloro-2-(diphenylmethyleneamino)pyridin-4(1H)-one is known for its potential applications in various scientific and industrial fields.
Uses
Used in Pharmaceutical and Agrochemical Industries:
(3-Chloro-2-(diphenylmethyleneamino)pyridin-4(1H)-one is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to be a versatile building block for the development of new drugs and pesticides.
Used as an Antifungal and Antibacterial Agent:
(3-Chloro-2-(diphenylmethyleneamino)pyridin-4(1H)-one has been studied for its potential use as an antifungal and antibacterial agent. Its ability to inhibit the growth of fungi and bacteria makes it a promising candidate for use in medical and agricultural applications.
Used in Organic Chemistry:
(3-Chloro-2-(diphenylmethyleneamino)pyridin-4(1H)-one has been investigated for its potential application in the field of organic chemistry. It serves as a valuable building block in the synthesis of complex organic molecules, contributing to the advancement of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 1174046-74-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,0,4 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1174046-74:
(9*1)+(8*1)+(7*7)+(6*4)+(5*0)+(4*4)+(3*6)+(2*7)+(1*4)=142
142 % 10 = 2
So 1174046-74-2 is a valid CAS Registry Number.
1174046-74-2Relevant articles and documents
The development of a scalable, chemoselective nitro reduction
Gallagher, William P.,Marlatt, Mark,Livingston, Robert,Kiau, Susanne,Muslehiddinoglu, Jale
, p. 1665 - 1668 (2013/02/23)
We have demonstrated a scalable chemoselective reduction of a nitro functional group in the presence of an aryl imine using (NH4) 2S/EtOH or hydrogenation (Sponge Nickel) to afford the corresponding amino-imines in moderate to excellent yields. Other reducible groups such as aryl halides, styryl olefins, and ether linkages survived as well.
