78024-39-2 Usage
Molecular structure
1-tert-butyl-2-(diethylamino)-4-oxo-3-phenylcyclobut-2-ene-1-carbonitrile has a complex molecular structure that includes a tert-butyl group, a diethylamino group, a carbonitrile functional group, and a cyclobutene ring with a phenyl substituent.
Physical properties
This chemical compound is a yellow solid, which indicates its appearance and stability in solid form.
Uses
1-tert-butyl-2-(diethylamino)-4-oxo-3-phenylcyclobut-2-ene-1-carbonitrile is used in organic synthesis and medicinal chemistry, which highlights its importance in the development of new molecules and materials.
Potential applications
Due to its unique structure and properties, this chemical compound has potential applications in pharmaceuticals and agrochemicals, indicating its possible use in the development of new drugs and chemicals for agriculture.
Reactivity
1-tert-butyl-2-(diethylamino)-4-oxo-3-phenylcyclobut-2-ene-1-carbonitrile may undergo various reactions and transformations in the presence of different reagents and conditions, making it a versatile building block in the development of new molecules and materials. This demonstrates its adaptability and usefulness in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 78024-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,2 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78024-39:
(7*7)+(6*8)+(5*0)+(4*2)+(3*4)+(2*3)+(1*9)=132
132 % 10 = 2
So 78024-39-2 is a valid CAS Registry Number.
78024-39-2Relevant academic research and scientific papers
(Aminoethynyl)metallations, IX. Reactions of Ynamines with Cyanoketenes
Himbert, Gerhard,Henn, Lothar
, p. 218 - 225 (2007/10/02)
Ynamines 2 bearing methyl or phenyl groups at their C/C triple bond react with tert-butylcyanoketene 1a to give the cyclobutenones 3 and/or the allene carboxamides 4. 3 and 4 are the products of two different cycloaddition reactions. β-Silylated, β-germylated and β-stannylated ynamines 5 add the cyanoketenes 1 under "(aminoethynyl)metallation" to furnish the new enynamines 6.These compounds were characterized by IR and 1H NMR spectroscopy and partly by mass spectrometry.The stannyl derivatives of 6 hydrolyze very easily to the corresponding acyl ynamines 7 and react with 4-nitrobenzoyl chloride to give the 1-(aminoethynyl)vinyl benzoates 8.The diazo compound 9 is formed by the interaction of tosyl azide on the enynamine 6c, which is probably first hydrolyzed to 7a.N,N-Diethyl-N-(triphenylsilylethynyl)amine (5e) reacts with two molecules of tert-butylcyanoketene (1a) to give the allene derivative 10, probably via the corresponding enynamine 6 (R1=R2=Et, MR33=SiPh3, R4=tBu). - Keywords: Ynamines, Cyanoketenes, Cycloaddition, (Aminoethynyl)metallation, (3-Alken-1-inyl)amines
