91091-11-1 Usage
Uses
Used in Pharmaceutical Synthesis:
DMAPN is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications. Its unique chemical structure allows for its use in creating a wide range of pharmaceutical compounds.
Used in Dye Manufacturing:
In the dye industry, DMAPN serves as a crucial intermediate, enabling the production of various dyes with different color properties and applications.
Used in Agricultural Chemicals:
DMAPN is also employed in the manufacturing of agricultural chemicals, where it plays a significant role in the development of products that enhance crop protection and yield.
Used in Organic Synthesis as a Chemical Reagent:
As a chemical reagent, DMAPN is involved in organic synthesis processes, facilitating the creation of new compounds and materials with diverse applications.
Used in Materials Science:
DMAPN has been studied for its potential applications in materials science, particularly as a component in organic semiconductors and dye-sensitized solar cells. Its inclusion in these technologies could lead to advancements in energy production and electronic devices.
Used as a Metal Corrosion Inhibitor:
DMAPN has been investigated for its potential use as an inhibitor for metal corrosion, which could have significant implications for the preservation and maintenance of various metal structures and components.
Check Digit Verification of cas no
The CAS Registry Mumber 91091-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,9 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91091-11:
(7*9)+(6*1)+(5*0)+(4*9)+(3*1)+(2*1)+(1*1)=111
111 % 10 = 1
So 91091-11-1 is a valid CAS Registry Number.
91091-11-1Relevant academic research and scientific papers
Lipilin,Churakov,Ioffe,Strelenko,Tartakovsky
, p. 596 - 598 (1997)
para-Nitroso-N,N-dimethylaniline reacts with tetracyanoethylene to give [4-(dimethylamino)phenylimino]malononitrile N-oxide 1 (65%) in addition to [4-(dimethylamino)phenylimino]malononitrile 2 (17%). The structures of the products are confirmed by spectra
Lithium bromide catalyzed Ehrlich-Sachs reactions using solvent-free conditions
Laskar,Prajapati,Sandhu
, p. 1427 - 1432 (2007/10/03)
Lithium bromide proves to be an efficient catalyst for Ehrlich-Sachs reaction of nitroso arenes with active methylene compounds under microwave irradiation through simple solvent-free reaction conditions.
Diimine-Tetracyanoethylene Donor-Acceptor Interactions: Synthesis of Pyrroles, Imidazolidines and Quinolines
Hassan, Alaa A.,Aly, Ashraf A.,Mohamed, Nasr K.,Mourad, Aboul-Fetouh E.
, p. 208 - 209 (2007/10/03)
N,N′-Bis(aryl)- (1) and N,N′-bis(cyclohexyl)-ethane-1,2-diylidenediamines (2) as well as N,N′-bis(aryl)benzene-1,4-diyldimethylidenediamines (3) reacted with tetracyanoethylene to give the title products.
REACTION OF DICYANOMETHYLENE COMPOUNDS WITH NITROSOARYLS
Bespalov, B. P.,Abolin, A. G.,Bel'skii, V. K.,Zavodnik, V. E.,Sobolev, A. N.,Chetkina, L. A.
, p. 720 - 727 (2007/10/02)
With nitrosoaryls tetracyanoethylene, tetracyanoquinodimethane, and 2-dicyanomethyleneindane-1,3-dione gives small yields of the corresponding dicyanomethylene anils.With 1-dicyanomethyleneindan-3-one and 1,3-bis(dicyanomethylene)indane in polar solvents
