106813-53-0 Usage
Chemical class
Ketone derivative
Explanation
1-Propanone, 1-(1-cyclohexen-1-yl)-3-phenyl-3-(phenylamino)is a complex ketone derivative, which means it is an organic compound with a carbonyl group (C=O) bonded to two carbon atoms, one of which is part of a cyclohexene ring.
Explanation
The compound contains a cyclohexene ring, which is a six-carbon ring with one double bond, and a phenylamino group, which is a phenyl ring (a six-carbon ring with alternating single and double bonds) bonded to a nitrogen atom.
Explanation
1-Propanone, 1-(1-cyclohexen-1-yl)-3-phenyl-3-(phenylamino)is commonly used as an intermediate in organic synthesis, meaning it is a starting material or a product in a multi-step chemical reaction that leads to the formation of a desired compound.
Explanation
Due to its unique structure and reactivity, the compound may have potential applications in various fields, such as pharmaceuticals (for the development of new drugs), agrochemicals (for the production of pesticides and fertilizers), and other industrial processes.
Explanation
The compound's complex structure and potential reactivity make it of interest to researchers, who may study its properties and potential applications further.
Explanation
The precise uses and properties of 1-Propanone, 1-(1-cyclohexen-1-yl)-3-phenyl-3-(phenylamino)would depend on the outcomes of ongoing research and development efforts, which may lead to the discovery of new applications and uses for 1-Propanone, 1-(1-cyclohexen-1-yl)-3-phenyl-3-(phenylamino)-.
Structure
Cyclohexene ring and phenylamino group
Usage
Intermediate in organic synthesis
Potential applications
Pharmaceuticals, agrochemicals, and industrial processes
Research interest
Unique structure and reactivity
Commercial applications
Dependent on research and development
Check Digit Verification of cas no
The CAS Registry Mumber 106813-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,1 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106813-53:
(8*1)+(7*0)+(6*6)+(5*8)+(4*1)+(3*3)+(2*5)+(1*3)=110
110 % 10 = 0
So 106813-53-0 is a valid CAS Registry Number.
106813-53-0Relevant academic research and scientific papers
High degree of exo selectivity in imino Diels-Alder reactions catalyzed by tert-butyldimethylsilyltriflate
Nogue,Paugam,Wartski
, p. 1265 - 1268 (2007/10/02)
Diels-Alder reactions of silyloxydiene 1 derived from 1-acetylcyclohexene with imines 2b and 2c occur with high exo selectivity depending upon experimental conditions: exo cycloadducts 3b-c are exclusively formed under kinetic control using tert-butyldime
Synthesis of 2-Phenyldecahydroquinolin-4-ones via Imino Diels-Alder Reaction: Influence of the Imine Nitrogen Substituent on the Reaction Course and on the Heterocycle Conformation
Coz, Linda Le,Veyrat-Martin, Christine,Wartski, Lya,Seyden-Penne, Jacqueline,Bois, Claudette,Philoche-Levisalles, Michele
, p. 4870 - 4879 (2007/10/02)
Reaction of acetylcyclohexene trimethylsilyl enol ether (1) with N-substituted phenyl imines 2 takes place in the presence of Lewis acids.When the N-substituent in 2 is phenyl, p-tolyl, or p-methoxyphenyl, the cycloaddition gives exo and endo enoxysilanes
STEREOSELECTIVE SYNTHESIS OF CIS OR TRANS N-PHENYL 2-PHENYL DECAHYDROQUINOLIN-4 ONES BY CATALYZED HETERO-DIELS-ALDER REACTION.
Veyrat, Christine,Wartski, Lya,Seyden-Penne, Jacqueline
, p. 2981 - 2984 (2007/10/02)
Cis or trans N-phenyl 2-phenyl decahydroquinolin-4 ones can be synthesized highly selectively.
