17627-44-0 Usage
Description
6-methyl-2-(4-methylcyclohex-3-enyl)hept-2,5-diene is an acyclic hydrocarbon, a type of organic compound characterized by its long chain structure with eight carbon atoms. 6-methyl-2-(4-methylcyclohex-3-enyl)hept-2,5-diene features two double bonds and a cyclohexene ring, along with methyl groups, which contribute to its unique chemical properties. It is primarily recognized for its role as a precursor in the synthesis of other organic compounds, with potential applications in chemistry and pharmaceuticals.
Uses
Used in Chemical Synthesis:
6-methyl-2-(4-methylcyclohex-3-enyl)hept-2,5-diene is used as a precursor in the chemical synthesis industry for the production of various organic compounds. Its unique structure, including the cyclohexene ring and double bonds, allows for versatile reactions and the creation of a wide range of derivatives.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 6-methyl-2-(4-methylcyclohex-3-enyl)hept-2,5-diene is utilized as a building block for the development of new pharmaceutical agents. Its potential applications may include the synthesis of novel drugs or the modification of existing ones to improve their efficacy, stability, or other pharmacological properties.
Used in Research and Development:
6-methyl-2-(4-methylcyclohex-3-enyl)hept-2,5-diene is also employed in research and development settings, where it can be used to study the properties of acyclic hydrocarbons and their derivatives. This can lead to a better understanding of their behavior in various chemical reactions and their potential applications in different fields.
The specific uses of 6-methyl-2-(4-methylcyclohex-3-enyl)hept-2,5-diene may vary depending on the context and the specific requirements of the application, highlighting its versatility and potential in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17627-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,2 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17627-44:
(7*1)+(6*7)+(5*6)+(4*2)+(3*7)+(2*4)+(1*4)=120
120 % 10 = 0
So 17627-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6-8,15H,5,9-11H2,1-4H3
17627-44-0Relevant articles and documents
Heteropoly acid catalyzed cyclization of nerolidol and farnesol: Synthesis of α-bisabolol
De Meireles, Augusto L.P.,Costa, Maíra Dos Santos,Da Silva Rocha, Kelly A.,Gusevskaya, Elena V.
, p. 271 - 275 (2015/07/07)
Heteropoly acid H3PW12O40 is an active and environmentally friendly homogeneous catalyst for the synthesis of α-bisabolol, a high-priced and highly demanded ingredient for the fragrance, cosmetic and pharmaceutical industries, starting from more abundant biomass-based sesquiterpenic alcohols. The solvent nature remarkably affects the reaction pathways and product selectivity. In acetone solutions, α-bisabolol can be obtained in 55-60% GC yields from nerolidol and 60-70% GC yields from farnesol at complete substrate conversions, which are probably the best results ever reported for these reactions. α-Bisabolol synthesized by this method contains no farnesol, which is a potentially allergenic compound and should be avoided in the commercially used α-bisabolol. This advantage is especially important because the distillative separation of α-bisabolol and farnesol is a troublesome task. The catalyst shows high turnover numbers and operates under mild nearly ambient conditions.
CYCLIZATION OF SOME LINEAR TERPENOLS INITIATED BY "ACTIVATED" DMSO
Surkova, A. A.,Lozanova, A. V.,Dragan, V. A.,Gur'yan, V. A.,Moiseenkov, A. M.
, p. 760 - 762 (2007/10/02)
It was shown that the acylhydroxysulfonium salt generated in situ from DMSO and trifluoroacetic anhydride causes low-temperature cyclization of geraniol, linalool, and nerol in an aprotic medium to a mixture of p-menthane monoterpenoids, and the maximum yield is obtained in the case of the last two terpenols.A similar result was obtained for E-nerolidol.
