1460-97-5 Usage
Uses
Used in Pharmaceutical Industry:
[1R,(-)]-1,2,3,4,4aα,5,6,8aβ-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene is used as an active pharmaceutical ingredient for the development of new drugs. Its unique molecular structure allows it to interact with specific biological targets, making it a promising candidate for the treatment of various diseases.
Used in Chemical Industry:
In the chemical industry, [1R,(-)]-1,2,3,4,4aα,5,6,8aβ-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene can be used as a starting material for the synthesis of other complex organic compounds. Its versatile structure enables it to be modified and functionalized to create a wide range of products with different applications.
Used in Research and Development:
Due to its unique chemical properties, [1R,(-)]-1,2,3,4,4aα,5,6,8aβ-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene is also used in research and development for studying various chemical reactions and mechanisms. It can serve as a model compound for understanding the behavior of similar naphthalene-based molecules and their interactions with other molecules.
Used in Antioxidant Applications:
As an antioxidant agent, [1R,(-)]-1,2,3,4,4aα,5,6,8aβ-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene can be used to protect materials from oxidative damage. Its ability to neutralize free radicals and prevent oxidation makes it a valuable additive in various industries, such as the food, cosmetic, and plastic industries, to enhance the shelf life and stability of products.
Check Digit Verification of cas no
The CAS Registry Mumber 1460-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1460-97:
(6*1)+(5*4)+(4*6)+(3*0)+(2*9)+(1*7)=75
75 % 10 = 5
So 1460-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13-15H,4-8H2,1-3H3
1460-97-5Relevant academic research and scientific papers
Rinkel, Jan,Rabe, Patrick,Garbeva, Paolina,Dickschat, Jeroen S.
, p. 13593 - 13596 (2016)
Stereospecifically labelled precursors were subjected to conversion by seven bacterial sesquiterpene cyclases to investigate the stereochemistry of their initial 1,10-cyclisation-1,3-hydride shift cascades. Enzymes with products of known absolute configuration showed a coherent stereochemical course, except for (?)-α-amorphene synthase, for which the obtained results are better explained by an initial 1,6-cyclisation. The link between the absolute configuration of the product and the stereochemical course of the 1,3-hydride shifts enabled assignment of the absolute configurations of three enzyme products, which were confirmed independently through the absolute configuration of the common byproduct germacrene D-4-ol.
Burkhardt, Immo,Kreuzenbeck, Nina B.,Beemelmanns, Christine,Dickschat, Jeroen S.
, p. 3348 - 3355 (2019)
Three terpene synthases from the termite associated fungus Termitomyces were functionally characterized as (+)-intermedeol synthase, (-)-γ-cadinene synthase and (+)-germacrene D-4-ol synthase, with the germacrene D-4-ol synthase as the first reported enzyme that produces the (+)-enantiomer. The enzymatic mechanisms were thoroughly investigated by incubation with isotopically labeled precursors to follow the stereochemical courses of single reaction steps in catalysis. The role of putative active site residues was tested by site directed mutagenesis of a highly conserved tryptophan in all three enzymes and additional residues in (-)-γ-cadinene synthase that were identified by homology model analysis.
