33082-72-3 Usage
Chemical structure
Cyclic ether derivative with a spiro ring system
Explanation
The compound has a cyclic structure, meaning the atoms are arranged in a closed loop. It is an ether derivative, which means it contains an oxygen atom bonded to two carbon atoms. The spiro ring system consists of two rings connected by a shared carbon atom.
Explanation
The methyl group is a carbon atom with three hydrogen atoms attached to it. In 1,4-Dioxaspiro[4.5]dec-7-ene, 8-methyl-, it is connected to the 8th carbon atom in the spiro ring system, which influences the compound's reactivity and potential applications.
Explanation
Due to its unique structure, 1,4-Dioxaspiro[4.5]dec-7-ene, 8-methylis used as a starting material or intermediate in the synthesis of various pharmaceuticals and agrochemicals.
Explanation
As a reagent, 1,4-Dioxaspiro[4.5]dec-7-ene, 8-methylis used in various chemical reactions and experiments to study its properties and potential applications.
Explanation
The compound's structure, particularly the presence of the methyl group on the spiro ring, makes it a promising candidate for the development of new therapeutic agents or bioactive compounds with potential applications in medicine and biotechnology.
Presence of two oxygen atoms
Oxygen atoms are part of the spiro ring system
Presence of a methyl group
A methyl group (CH3) is attached to the 8th carbon atom
Application in organic synthesis
Building block for pharmaceuticals and agrochemicals
Utilization in material science
Potential applications in the development of new materials
Use as a reagent
Employed in chemical research
Potential for therapeutic agents or bioactive compounds
Unique structure makes it a candidate for new developments
Check Digit Verification of cas no
The CAS Registry Mumber 33082-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33082-72:
(7*3)+(6*3)+(5*0)+(4*8)+(3*2)+(2*7)+(1*2)=93
93 % 10 = 3
So 33082-72-3 is a valid CAS Registry Number.
33082-72-3Relevant academic research and scientific papers
A Pd-Catalyzed Site-Controlled Isomerization of Terminal Olefins
Ren, Wenlong,Sun, Fei,Chu, Jianxiao,Shi, Yian
supporting information, p. 1868 - 1873 (2020/03/03)
An effective Pd-catalyzed isomerization of olefins with 2-PyPPh2 as the ligand is described. A wide variety of trans-2-olefins bearing various functional groups can be obtained with high regio- A nd stereoselectivity under mild reaction conditions. The ligand is crucial for the reaction.
Construction of Distant Stereocenters by Enantioselective Desymmetrizing Carbonyl-Ene Reaction
Luo, Weiwei,Lin, Lili,Zhang, Yu,Liu, Xiaohua,Feng, Xiaoming
, p. 3374 - 3377 (2017/07/15)
An efficient desymmetrizing carbonyl-ene reaction of 1-substituted 4-methylenecyclohexanes with glyoxal derivatives was thus executed by a chiral N,N′-dioxide/NiII catalyst, providing facile access to cyclohexene derivatives bearing two remote 1,6-related stereocenters. This distal stereocontrol methodology originates from the efficient interaction between the catalyst with enophiles, discrimination of the two chair conformations of olefinic components, and the intrinsic six-membered transition-state structure of ene process.
Synthesis of 3-Ethenyl-4-methyl-cyclohex-2-en-1-one from 4-Methylanisole
Burge, Geoffrey L.,Collins, David J.,Reitze, John D.
, p. 1913 - 1925 (2007/10/02)
Epoxidation of 8-methyl-1,4-dioxaspirodec-7-ene (13) with peroxybenzoic acid afforded 6'-methylspirooxabicycloheptane> (12), isomerization of which with a catalytic amount of lithium perchlorate in refluxing benzene yield
A NEW SYNTHON FOR THE REGIOSPECIFIC γ-ALKYLATION OF 2-CYCLOHEXENONES. APPLICATION TO THE SYNTHESIS OF ZINGIBERENOL AND OXYGENATED BICYCLONONANES
Paquette, Leo A.,Kinney, William A.
, p. 131 - 134 (2007/10/02)
The regiospecific γ-alkylation of γ-sulfonylcyclohexenone ketals is described and applied to various synthetic objectives.
