22556-08-7 Usage
Description
[1S-(1alpha,3beta,4alpha,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is a bicyclic organic compound characterized by its complex stereochemistry and the presence of four chiral centers. This molecule, with the molecular formula C10H18O2, is known for its biological activity and is a significant compound in pharmaceutical research. Its unique structure and properties make it a valuable target for further exploration in various scientific and medical fields.
Uses
Used in Pharmaceutical Research:
[1S-(1alpha,3beta,4alpha,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is used as a key compound in pharmaceutical research for its potential applications in medicine, drug development, and the production of functional materials. Its unique structure and biological properties make it an attractive candidate for the development of new therapeutic agents.
Used in Synthesis of Natural Products and Pharmaceuticals:
[1S-(1alpha,3beta,4alpha,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol serves as a starting material for the synthesis of various natural products and pharmaceuticals. Its versatility in chemical reactions and potential to be modified or functionalized makes it a valuable building block in the creation of new and improved drugs.
Used in Medicine:
[1S-(1alpha,3beta,4alpha,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is used as a biologically active molecule in the field of medicine. Its potential applications in medicine are currently under investigation, and its unique properties may lead to the development of novel treatments for various diseases and conditions.
Used in Drug Development:
In the process of drug development, this compound is used as a starting point for the design and synthesis of new pharmaceuticals. Its stereochemical complexity and biological activity make it a promising candidate for the development of innovative drugs with improved efficacy and selectivity.
Used in Production of Functional Materials:
The unique structure of [1S-(1alpha,3beta,4alpha,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol also lends itself to the production of functional materials with specific properties. These materials could have applications in various industries, such as electronics, coatings, and adhesives, where their unique characteristics can be harnessed for improved performance.
Check Digit Verification of cas no
The CAS Registry Mumber 22556-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,5 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22556-08:
(7*2)+(6*2)+(5*5)+(4*5)+(3*6)+(2*0)+(1*8)=97
97 % 10 = 7
So 22556-08-7 is a valid CAS Registry Number.
22556-08-7Relevant articles and documents
Sustainable catalytic protocols for the solvent free epoxidation and: Anti -dihydroxylation of the alkene bonds of biorenewable terpene feedstocks using H2O2 as oxidant
Cunningham, William B.,Tibbetts, Joshua D.,Hutchby, Marc,Maltby, Katarzyna A.,Davidson, Matthew G.,Hintermair, Ulrich,Plucinski, Pawel,Bull, Steven D.
supporting information, p. 513 - 524 (2020/02/13)
A tungsten-based polyoxometalate catalyst employing aqueous H2O2 as a benign oxidant has been used for the solvent free catalytic epoxidation of the trisubstituted alkene bonds of a wide range of biorenewable terpene substrates. This epoxidation protocol has been scaled up to produce limonene oxide, 3-carene oxide and α-pinene oxide on a multigram scale, with the catalyst being recycled three times to produce 3-carene oxide. Epoxidation of the less reactive disubstituted alkene bonds of terpene substrates could be achieved by carrying out catalytic epoxidation reactions at 50 °C. Methods have been developed that enable direct epoxidation of untreated crude sulfate turpentine to afford 3-carene oxide, α-pinene oxide and β-pinene oxide. Treatment of crude epoxide products (no work-up) with a heterogeneous acid catalyst (Amberlyst-15) results in clean epoxide hydrolysis to afford their corresponding terpene-anti-diols in good yields.
Syntheses of the optically active terpene hydroxyphenylselenides
Scianowski, Jacek,WeLniak, MirosLaw
scheme or table, p. 1440 - 1447 (2010/03/24)
The optically active hydroxyphenylselenides derived from the p-menthane, carane, and pinane systems have been obtained. Two methods of hydroxyphenylselenides synthesis have been compared. The first method is based on the reaction of alkenes with N-(phenylseleno)succinimide in the presence of water, and the second from epoxides as a result of the reaction with sodium benzeneselenolate. The influence of the substrate structures on the composition of the obtained products has been demonstrated.
INTRODUCTION OF OXYGENATED FUNCTIONAL GROUPS INTO 3-CARENE AND 2-PINENE BY CULTURED CELLS
Hirata, Toshifumi,Ikeda, Yoshihiro,Izumi, Shunsuke,Shimoda, Kei,Hamada, Hiroki,Kawamura, Toshinari
, p. 401 - 404 (2007/10/02)
The biotransformation of the monoterpene hydrocarbons 3-carene and 2-pinene by cell suspension cultures of Nicotiana tabacum and Catharanthus roseus was investigated.The cultures have the ability to regio- and enantioselectively introduce the oxygenated functional groups into the C=C double bond and the allylic positions of the substrates. - Key words: Nicotiana tabacum; Solanaceae; Catharanthus roseus; Apocyanaceae; cultured cells; biotransformation; epoxidation; hydroxylation; carene; pinene.
