116425-36-6 Usage
General Description
2-Isopropylidene-6-methyl-5-(3-oxobutyl)-4-cyclohepten-1-one is a chemical compound with a complex structure, consisting of a cycloheptenone ring with an isopropylidene and methyl group attached, as well as a 3-oxobutyl side chain. 2-Isopropylidene-6-methyl-5-(3-oxobutyl)-4-cyclohepten-1-one is commonly used as a flavoring agent and fragrance in the food and cosmetic industries, and it exhibits a fruity and floral odor. It is also used in the synthesis of various organic compounds and pharmaceuticals. Additionally, it may have potential applications in medicine and research due to its unique chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 116425-36-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,2 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116425-36:
(8*1)+(7*1)+(6*6)+(5*4)+(4*2)+(3*5)+(2*3)+(1*6)=106
106 % 10 = 6
So 116425-36-6 is a valid CAS Registry Number.
116425-36-6Relevant articles and documents
Structural diversity from the transannular cyclizations of natural germacrone and epoxy derivatives: A theoretical-experimental study
Pérez Morales, M. Carmen,Catalán, Julieta V.,Domingo, Victoriano,Jaraíz, Martín,Herrador, M. Mar,Quílez Del Moral, José F.,L?pez-Pérez, José-Luis,Barrero, Alejandro F.
supporting information, p. 6598 - 6612 (2013/06/27)
Treatment of germacrone (1) with different electrophiles, and of its epoxy derivatives germacrone-4,5-epoxide (2), germacrone-1,10-epoxide (3) and isogermacrone-4,5-epoxide (4) with Br?nsted/Lewis acids and Ti III, gives rise to a great structural diversity. Thus, by using a maximum of two steps, the production of more than 40 compounds corresponding to 14 skeletons is described. Computational calculations rationalizing the structural divergence produced are also described. Finally, since some of the compounds generated are bioactive natural sesquiterpenes, the mechanisms of formation of these substances will provide new insights in their biosynthesis. Copyright
