69962-41-0 Usage
Description
3-(N,N-Diallyl)aminoacetanilide is a chemical compound that belongs to the class of organic compounds, specifically anilides and derivatives. It is represented by the chemical formula C14H20N2O. 3-(N,N-Diallyl)aminoacetanilide is primarily used in research and experimental settings, and its properties such as melting point, boiling point, and density may vary. It is important to refer to the supplier's details or scientific research for accurate information. Due to potential biohazard or toxicity risks, care should be taken in its handling and usage.
Uses
Used in Research and Experimental Settings:
3-(N,N-Diallyl)aminoacetanilide is used as a chemical compound in research and experimental settings for various scientific investigations. Its specific applications may include the study of chemical reactions, synthesis of new compounds, or as a reference material in analytical chemistry.
Used in Pharmaceutical Research:
3-(N,N-Diallyl)aminoacetanilide is used as a potential pharmaceutical candidate in the development of new drugs. Its chemical structure and properties may be of interest to researchers exploring its potential therapeutic applications, such as in the treatment of diseases or as a component in drug formulations.
Used in Chemical Synthesis:
3-(N,N-Diallyl)aminoacetanilide is used as a starting material or intermediate in the synthesis of other chemical compounds. Its reactivity and functional groups may be utilized in the preparation of more complex molecules or in the development of new chemical processes.
Used in Analytical Chemistry:
3-(N,N-Diallyl)aminoacetanilide is used as a reference material or standard in analytical chemistry for the calibration of instruments or the validation of analytical methods. Its well-defined chemical structure and properties make it suitable for such applications, ensuring accurate and reliable results in chemical analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 69962-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,6 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69962-41:
(7*6)+(6*9)+(5*9)+(4*6)+(3*2)+(2*4)+(1*1)=180
180 % 10 = 0
So 69962-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O/c1-4-9-16(10-5-2)14-8-6-7-13(11-14)15-12(3)17/h4-8,11H,1-2,9-10H2,3H3,(H,15,17)
69962-41-0Relevant articles and documents
A Phosphine-Mediated Dearomative Skeletal Rearrangement of Dianiline Squaraine Dyes
Bacher, Emily P.,Koh, Kevin J.,Lepore, Antonio J.,Oliver, Allen G.,Wiest, Olaf,Ashfeld, Brandon L.
supporting information, p. 2853 - 2857 (2021/05/05)
A phosphorus(III)-mediated dearomatization of ortho-substituted dianiline squaraine dyes results in an unusual skeletal rearrangement to provide exotic, highly conjugated benzofuranone and oxindole scaffolds bearing a C3 side chain comprised of a linear conflagration of an enol, a phosphorus ylide, and 2,4-disubstituted aniline. Employing experimental and computational analysis, a mechanistic evaluation revealed a striking dependence on the acidity of the aniline ortho substituent. Notably, the rearrangement adducts underwent rapid and complete reversion to the parent squaraine in the presence of a Br?nsted acid.
Assisted tandem catalytic RCM-aromatization in the synthesis of pyrroles and furans
Schmidt, Bernd,Krehl, Stefan,Jablowski, Eric
supporting information; experimental part, p. 5119 - 5130 (2012/08/07)
An assisted tandem catalytic transformation of diallyl amines and diallyl ethers into N-aryl pyrroles and furans, respectively, is described. The sequence relies on ring closing metathesis followed by dehydrogenation of the initially formed dihydropyrroles and dihydrofurans. Both steps are Ru-catalyzed, but the sequence requires only one precatalyst, because conversion of the metathesis catalyst into the dehydrogenation catalyst is achieved in situ, triggered by the oxidant tert-butyl hydroperoxide.
