52645-90-6 Usage
Description
(4aS,6aS,8S,11aS,11bS)-4,4,9,11b-tetramethyl-1,2,3,4,4a,5,6,6a,7,8,11,11b-dodecahydro-8,11a-methanocyclohepta[a]naphthalene is a complex chemical compound belonging to the class of terpenes. It is characterized by a unique molecular structure with a fused polycyclic ring system and four methyl groups. (4aS,6aS,8S,11aS,11bS)-4,4,9,11b-tetramethyl-1,2,3,4,4a,5,6,6a,7,8,11,11b-dodecahydro-8,11a-methanocyclohepta[a]naphthalene is typically found in essential oils and plant resins, and due to its specific arrangement of carbon atoms, it falls under the category of cycloalkanes, which are saturated hydrocarbons.
Uses
Used in Organic Chemistry:
(4aS,6aS,8S,11aS,11bS)-4,4,9,11b-tetramethyl-1,2,3,4,4a,5,6,6a,7,8,11,11b-dodecahydro-8,11a-methanocyclohepta[a]naphthalene is used as a key intermediate for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmacology:
In the field of pharmacology, this compound serves as a valuable building block for the development of new drugs. Its specific configuration and properties can be exploited to design molecules with targeted therapeutic effects.
Used in Fragrance Production:
(4aS,6aS,8S,11aS,11bS)-4,4,9,11b-tetramethyl-1,2,3,4,4a,5,6,6a,7,8,11,11b-dodecahydro-8,11a-methanocyclohepta[a]naphthalene is used as a base material for creating unique and complex fragrances. Its presence in essential oils and plant resins makes it a natural choice for the perfumery industry.
Used in the Chemical Industry:
(4aS,6aS,8S,11aS,11bS)-4,4,9,11b-tetramethyl-1,2,3,4,4a,5,6,6a,7,8,11,11b-dodecahydro-8,11a-methanocyclohepta[a]naphthalene is also utilized in the chemical industry for various applications, such as the production of specialty chemicals, coatings, and adhesives. Its unique structure and properties make it a versatile component in the development of new materials with specific characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 52645-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,4 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52645-90:
(7*5)+(6*2)+(5*6)+(4*4)+(3*5)+(2*9)+(1*0)=126
126 % 10 = 6
So 52645-90-6 is a valid CAS Registry Number.
52645-90-6Relevant articles and documents
Biosynthesis of diterpenoid aphidicolin: Isolation of intermediates from P-450 inhibitor treated mycelia of Phoma betae
Oikawa, Hideaki,Ohashi, Satoshi,Ichihara, Akitami,Sakamura, Sadao
, p. 7541 - 7554 (2007/10/03)
Treatment of Phoma betae with P-450 inhibitors caused accumulation of biosynthetic precursors 2, 3 and 4 of aphidicolin (1). Their structures were elucidated by spectroscopic analysis and they were confirmed by chemical transformations from 1. Isotopicall
