201423-75-8 Usage
Molecular Structure
The compound consists of a cyclohexanone ring with an allyloxymethyl functional group attached at the 2-position.
Functional Groups
Contains a ketone group (C=O) and an allyl group (C3H5-).
Usage
Can be used as a starting material in organic synthesis for the preparation of various other organic compounds.
Industry Applications
Has potential applications in the pharmaceutical, agrochemical, and polymer industries.
Chemical Reactivity
The allyloxymethyl group can undergo various chemical reactions, such as oxidation, reduction, and substitution, leading to the synthesis of a wide range of derivatives with diverse properties.
Safety Precautions
Proper handling and safety precautions should be observed when working with 2-(allyloxymethyl)cyclohexanone.
Check Digit Verification of cas no
The CAS Registry Mumber 201423-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,2 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 201423-75:
(8*2)+(7*0)+(6*1)+(5*4)+(4*2)+(3*3)+(2*7)+(1*5)=78
78 % 10 = 8
So 201423-75-8 is a valid CAS Registry Number.
201423-75-8Relevant academic research and scientific papers
Sequential Ketyl-Olefin Coupling/β-Elimination Reactions Mediated by Samarium(II) Iodide
Molander, Gary A.,Harris, Christina R.
, p. 812 - 816 (2007/10/03)
Samarium(II) iodide (SmI2) has been employed in an intramolecular sequential ketyl-olefin coupling/β-elimination reaction. The overall process results in the net addition of an alkenyl species to a ketone carbonyl. This novel protocol for the intramolecular delivery of an alkenyl moiety avoids the basic reaction conditions typical of nucleophilic additions that are mediated by alkenylmagnesium halides and alkenyllithium reagents. A high degree of stereocontrol is imparted in the SmI2-mediated process as a result of the excellent facial selectivity conveyed in the initial ketyl-olefin coupling reaction. The relative asymmetric induction engendered in these addition reactions is complementary to more traditional nucleophilic addition reactions in that the alkenyl group is directed to the carbonyl center by an attached tether.
