799813-25-5 Usage
Chemical Class
Terpenoid
A type of organic compound that is derived from isoprene units.
Core Structure
Naphthalene
A polycyclic aromatic hydrocarbon with two fused benzene rings.
Substituents
Methyl and Isopropyl groups
Methyl (CH3) and isopropyl (CH3CH(CH3)) are alkyl groups attached to the core structure.
Compound Type
Cyclic Ketone
A type of ketone with a ring structure and a carbonyl group (C=O) within the ring.
Specific Stereochemistry
1R, 7R, 8aR
The stereochemistry indicates the spatial arrangement of the substituents on the molecule, which is important for its properties and applications.
Family
Naphthoquinones
A group of organic compounds with a naphthalene core and a ketone functional group.
Potential Uses
Pharmaceuticals, Fragrances, and Pesticides
The compound may have applications in various industries due to its unique structure and properties.
Further Research
Necessary for full understanding of characteristics and uses
More studies and analysis are required to explore the properties and potential applications of this complex chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 799813-25-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,8,1 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 799813-25:
(8*7)+(7*9)+(6*9)+(5*8)+(4*1)+(3*3)+(2*2)+(1*5)=235
235 % 10 = 5
So 799813-25-5 is a valid CAS Registry Number.
799813-25-5Relevant articles and documents
Eremophilane sesquiterpenes from capsidiol
Zhao, Yuxin,Schenk, David J.,Takahashi, Shunji,Chappell, Joe,Coates, Robert M.
, p. 7428 - 7435 (2007/10/03)
A series of eremophilane sesquiterpene alcohols and hydrocarbons was prepared from the phytoalexin capsidiol (1) for mechanistic studies with epiaristolochene synthase and epiaristolochene dihydroxylase. Among them, 3-deoxycapsidiol (10) was obtained through selective derivatization and reductive cleavage of the equatorial 3α hydroxyl group. Two novel isomers of aristolochene and eremophilene were accessed from the 1- and 3-deoxycapsidiol isomers. 4-Epieremophilene (17) was obtained by conjugate reduction of epiaristolochen-1-one tosylhydrazone with catecholborane followed by sulfinate elimination and diimide rearrangement. Epimerization of epiaristolochen-3-one (27a) at the C4 methyl followed by reductions led to the previously unknown aristolochene isomer, eremophila-9(10),11(12)-diene (30). Optical rotations and characteristic 1H NMR data for the related eremophilenols and dienes are collected in Tables 1 and 2. Finally, bioassays were used to assess the antifungal potencies of capsidiol and its synthetic derivatives. The minimum inhibitory concentration for capsidiol (3-10 ng) was at least 1 order of magnitude lower than that of any of the derivatives and considerably lower than those previously reported for ketoconazole, nystatin, and propiconazole.
