74690-89-4 Usage
Uses
Used in Pharmaceutical Industry:
3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester is used as a pharmaceutical compound for its potential therapeutic applications. Its complex structure may offer unique interactions with biological systems, making it a candidate for the development of new drugs or drug delivery systems.
Used in Fragrance Industry:
In the fragrance industry, 3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester is used as a scent ingredient. Its specific chemical composition may contribute to the creation of novel fragrances or enhance existing ones, providing a distinct olfactory profile.
Used in Chemical Research:
3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester is utilized in chemical research as a subject of study for its unique structural features and potential reactivity. Researchers may explore its properties to gain insights into new chemical reactions or to develop innovative applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 74690-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,9 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74690-89:
(7*7)+(6*4)+(5*6)+(4*9)+(3*0)+(2*8)+(1*9)=164
164 % 10 = 4
So 74690-89-4 is a valid CAS Registry Number.
74690-89-4Relevant academic research and scientific papers
Fukuyama, Yoshiyasu,Minami, Hiroyuki,Takaoka, Shigeru,Kodama, Mitsuaki,Kawazu, Kazuyoshi,Nemoto, Hisao
, p. 1435 - 1438 (1997)
The absolute structure of vibsanin C, a novel 7-membered vibsane-type diterpene isolated from the leaves of Viburnum awabuki, has been established by X-ray crystallographic analysis of its derivative. Vibsanin C has been proved to be one of Cope rearranged products from vibsanin B, a 11-membered vibsane-type diterpene.
Synthesis and neurite outgrowth promoting activity of vibsanin B derivatives
Shao, Li-Dong,Xu, Jun,Gao, Xiu,He, Juan,Zhao, Yu,Peng, Li-Yan,Luo, Huai-Rong,Xia, Chengfeng,Zhao, Qin-Shi
supporting information, p. 3414 - 3417 (2014/06/09)
Intramolecular hetero-DA reaction and unexpected retro-aldol like ring opening reaction were performed. As a result, six derivatives with different skeletons of vibsane-type diterpenoids were synthesized from vibsanin B within three steps. Moreover, compounds 2, 3, and 6 enhanced the neurite outgrowth of NGF-mediated PC12 cells.
