52645-90-6 Usage
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, (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 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 academic research and scientific papers
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
