74598-74-6 Usage
Description
Methanone, 1-cyclohexen-1-ylcyclohexyl-, also known as Cyclohexyl-1-cyclohexenyl Ketone, is an organic compound with a ketone functional group. It consists of a cyclohexenyl group attached to a cyclohexyl group through a carbonyl linkage. Methanone, 1-cyclohexen-1-ylcyclohexylis known for its unique chemical properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
Methanone, 1-cyclohexen-1-ylcyclohexylis used as an intermediate in the synthesis of enones, which are important building blocks in the preparation of various pharmaceutical compounds. Methanone, 1-cyclohexen-1-ylcyclohexylis utilized in the nickel-catalyzed carbonylative Negishi cross-coupling reaction to produce enones with specific structural features, enabling the development of novel drugs with improved therapeutic properties.
Used in Chemical Synthesis:
In the field of organic chemistry, Methanone, 1-cyclohexen-1-ylcyclohexylserves as a versatile intermediate for the synthesis of various organic compounds. Methanone, 1-cyclohexen-1-ylcyclohexyl-'s unique structure allows for a wide range of chemical reactions, such as cross-coupling, oxidation, and reduction, enabling the creation of diverse chemical libraries for research and development purposes.
Used in Material Science:
Methanone, 1-cyclohexen-1-ylcyclohexylcan also be employed in the development of advanced materials with specific properties. Methanone, 1-cyclohexen-1-ylcyclohexyl-'s ability to participate in various chemical reactions allows for the synthesis of novel polymers, coatings, and other materials with tailored characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 74598-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,9 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74598-74:
(7*7)+(6*4)+(5*5)+(4*9)+(3*8)+(2*7)+(1*4)=176
176 % 10 = 6
So 74598-74-6 is a valid CAS Registry Number.
74598-74-6Relevant articles and documents
Enones from Acid Fluorides and Vinyl Triflates by Reductive Nickel Catalysis
Pan, Feng-Feng,Guo, Peng,Li, Chun-Ling,Su, Peifeng,Shu, Xing-Zhong
supporting information, p. 3701 - 3705 (2019/05/24)
A nickel-catalyzed reductive coupling between acid fluorides and vinyl triflates has been described. This method provides an efficient access to various enones and avoids the requirement for acyl or vinyl metallic reagents in the conventional approaches.
Some novel routes to 1-heterosubstituted 1-vinylcyclopropanes
Lewis, Richard T.,Motherwell, William B.
, p. 1465 - 1484 (2007/10/02)
3-Phenylselenoalk-1-enylidene carbenes, generated in situ by base induced condensation of α-phenylseleno carbonyl compounds and diethyl diazomethylphosphonate, can be efficiently trapped by alkenes to give alkylidene-cyclopropane adducts which undergo either [1,3] allyl selenide rearrangement or oxidative selenoxide [2,3] sigmatropic rearrangement to produce 1-phenylseleno- or 1-hydroxy-1-vinylcyclopropanes respectively.
Generation, Trapping, and Adduct Rearrangement of 3-Phenylselenoalk-1-enylidene Carbenes: a Novel Direct Route to 1-Hetero-substituted 1-Vinylcyclopropanes
Lewis, Richard T.,Motherwell, William B.
, p. 751 - 753 (2007/10/02)
3-Phenylselenoalk-1-enylidene carbenes, generated in situ by base-induced Horner-Wadsworth-Emmons condensation of α-phenylseleno carbonyl compounds and diethyl diazomethylphosphonate, may be efficiently trapped to give alkylidene-cyclopropane adducts which undergo either allyl selenide rearrangement or oxidative selenoxidesigmatropic rearrangement to produce 1-heterosubstituted 1-vinylcyclopropanes.