7063-68-5 Usage
Uses
Used in Pharmaceutical Industry:
CYCLOPENTYL 2-METHOXYPHENYL KETONE is used as a chemical intermediate for the synthesis of various pharmaceuticals and organic compounds. Its versatile reactivity and ability to form different chemical bonds make it a valuable component in creating a range of medicinal products.
Used in Chemical Industry:
In the chemical industry, CYCLOPENTYL 2-METHOXYPHENYL KETONE is utilized as a key intermediate in the production of a variety of organic compounds. Its unique structure and reactivity contribute to the development of new chemical entities with potential applications in various fields.
Used in Research and Development:
CYCLOPENTYL 2-METHOXYPHENYL KETONE is used as a research compound for studying its potential biological activities, such as anti-inflammatory and anti-cancer properties. This research can lead to the discovery of new therapeutic agents and contribute to advancements in medical science.
Used in Drug Development:
Due to its potential biological activities, CYCLOPENTYL 2-METHOXYPHENYL KETONE is employed in drug development as a starting material for creating new pharmaceuticals with possible applications in treating inflammation and cancer. Its unique structure and reactivity allow for the exploration of novel therapeutic approaches.
Check Digit Verification of cas no
The CAS Registry Mumber 7063-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7063-68:
(6*7)+(5*0)+(4*6)+(3*3)+(2*6)+(1*8)=95
95 % 10 = 5
So 7063-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C26H28N4O2S2/c1-4-29-23(28-12-8-9-17(2)15-28)20(18(3)21(14-27)24(29)31)13-22-25(32)30(26(33)34-22)16-19-10-6-5-7-11-19/h5-7,10-11,13,17H,4,8-9,12,15-16H2,1-3H3
7063-68-5Relevant academic research and scientific papers
Direct catalytic asymmetric three-component Kabachnik-fields reaction
Cheng, Xu,Goddard, Richard,Buth, Gernot,List, Benjamin
supporting information; experimental part, p. 5079 - 5081 (2009/03/11)
(Chemical Equation Presented) As mimics of α-amino acids, α-amino phosphonates have great promise as antibacterial and anti-HIV agents as well as protease inhibitors. Racemic α-branched aldehydes react, in the presence the new chiral phosphoric acid catalyst 1, directly with p-anisidine (PMPNH2) and a phosphite to furnish β-branched α-amino phosphonates highly diastereoselectively and enantioselectively. Anth = anthracenyl.
Unexpected Migration and Oxidative Cyclization of Substituted 2-Acetophenone Triflates under Basic Conditions: Synthetic and Mechanistic Insights
Coe, Jotham W.,Bianco, Krista E.,Boscoe, Brian P.,Brooks, Paige R.,Cox, Eric D.,Vetelino, Michael G.
, p. 9964 - 9970 (2007/10/03)
Oxidative ring closure of alkyl-substituted 2-hydroxyacetophenone trifluoromethanesulfonate esters (triflates) occurs upon exposure to base in anaerobic DMF at 20-90 °C. Alkyl substitution is required for ring closure. A migrated enol triflate product forms at lower temperature in high yield via migration of the trifluoromethanesulfonate in the unsubstituted and monoalkyl-substituted cases. The alkyl-substituted enol triflates also enter into the benzofuran-3-one ring-forming process under thermal cyclization conditions. Potential mechanistic pathways are evaluated.
