52645-90-6 Usage
General 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 chemical compound with a complex and lengthy molecular structure, featuring four methyl groups and a fused polycyclic ring system. It falls under the category of cycloalkanes, which are saturated hydrocarbons that form cyclical structures due to the arrangement of carbon atoms. This particular compound belongs to the class of terpenes and is commonly found in essential oils and plant resins. Due to its unique structure, it may have potential applications in the field of organic chemistry, pharmacology, and fragrance production. The chemical name specifies the exact arrangement and configuration of the atoms in the molecule, facilitating its identification and understanding of its properties and potential uses.
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
