56506-81-1 Usage
Description
(E,E)-Farnesol Benzyl Ether is a terpene derivative, characterized as a colorless oil. It is a naturally occurring compound that can be found in various plants and is known for its distinct chemical properties and potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
(E,E)-Farnesol Benzyl Ether is used as a key component in the preparation of essential coenzymes, such as coenzyme Q, vitamin K, and polyprenylquinones. These coenzymes play a crucial role in various biological processes, including cellular respiration and energy production, as well as blood clotting and bone metabolism.
(E,E)-Farnesol Benzyl Ether's presence in the pharmaceutical industry highlights its importance in the synthesis of vital molecules that contribute to maintaining overall health and well-being.
Used in Chemical Industry:
As a terpene derivative, (E,E)-Farnesol Benzyl Ether can also be utilized in the chemical industry for the development of various products, such as fragrances, flavors, and additives. Its unique chemical structure and properties make it a valuable component in the creation of diverse chemical compounds with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 56506-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,0 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56506-81:
(7*5)+(6*6)+(5*5)+(4*0)+(3*6)+(2*8)+(1*1)=131
131 % 10 = 1
So 56506-81-1 is a valid CAS Registry Number.
56506-81-1Relevant articles and documents
Chemoselective and stereoselective lithium carbenoid mediated cyclopropanation of acyclic allylic alcohols
Durán-Pe?a,Flores-Giubi,Botubol-Ares,Harwood,Collado,Macías-Sánchez,Hernández-Galán
, p. 2731 - 2741 (2016/03/05)
The reaction of geraniol with different lithium carbenoids generated from n-BuLi and the corresponding dihaloalkane has been evaluated. The reaction occurs in a chemo and stereoselective manner, which is consistent with a directing effect from the oxygen of the allylic moiety. Furthermore, a set of polyenes containing allylic hydroxyl or ether groups were chemoselectively and stereoselectively converted into the corresponding gem-dimethylcyclopropanes in one single step in moderate to good yields mediated by a lithium carbenoid generated in situ by the reaction of n-BuLi and 2,2-dibromopropane.
Regio- and Stereoselective Synthesis of 1,5-Dienes Using Allylic Barium Reagents
Yanagisawa, Akira,Hibino, Hiroaki,Habaue, Shigeki,Hisada, Yoshiyuki,Yasue, Katsutaka,Yamamoto, Hisashi
, p. 1263 - 1268 (2007/10/03)
The highly α,α' selective and sterocontrolled homocoupling reaction of allylic halides was achieved using barium reagent.The double-bond geometry of the starting allylic chloride was completely retained.The α,α' cross-coupling products were also prepared stereospecifically and regioselectively by this method.
