69807-62-1 Usage
General Description
1-benzoyl-2-(naphth-1-ylamino)ethene is a chemical compound with the molecular formula C20H15NO. It is a benzophenone derivative with a naphthylamine group attached to the ethene carbon. 1-benzoyl-2-(naphth-1-ylamino)ethene is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure and properties make it a valuable intermediate for creating new molecules with potential applications in drug discovery and development. Additionally, it can act as a fluorescence probe for studying biological systems and as a reagent in organic reactions. Overall, 1-benzoyl-2-(naphth-1-ylamino)ethene has diverse applications and is an important molecule in the field of organic and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 69807-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,0 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69807-62:
(7*6)+(6*9)+(5*8)+(4*0)+(3*7)+(2*6)+(1*2)=171
171 % 10 = 1
So 69807-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H15NO/c21-19(16-8-2-1-3-9-16)13-14-20-18-12-6-10-15-7-4-5-11-17(15)18/h1-14,20H/b14-13+
69807-62-1Relevant academic research and scientific papers
Silver(i)/base-promoted propargyl alcohol-controlled regio- or stereoselective synthesis of furan-3-carboxamides and (Z)-enaminones
Sultana, Sabera,Shim, Jae-Jin,Kim, Sung Hong,Lee, Yong Rok
, p. 6749 - 6759 (2018/09/29)
A novel and facile regioselective synthesis of furan-3-carboxamides by a silver(i)/base-promoted reaction of propargyl alcohol with 3-oxo amides has been demonstrated. This one-pot protocol provides a rapid synthetic approach to diverse trisubstituted furan-3-carboxamides via cascade nucleophilic addition, intramolecular cyclization, elimination, and isomerization reactions. Employing a substituted propargyl alcohol, (Z)-enaminones have been obtained with high stereoselectivities by a Ag2CO3-promoted reaction starting from 3-oxo amides via C-N bond cleavage.
Organocatalytic activation of isocyanides: N-heterocyclic carbene-catalyzed enaminone synthesis from ketones
Kim, Jungwon,Hong, Soon Hyeok
, p. 2401 - 2406 (2017/03/11)
The first example of the use of an N-heterocyclic carbene (NHC) as an organocatalyst for the activation of isocyanides was demonstrated. On the basis of previous reports on the interaction between NHCs and isocyanides, we developed a catalytic cycle invol
