800385-98-2 Usage
Description
1(2H)-Naphthalenone,3,4,4a,5,6,7-hexahydro-4,4a-dimethyl-6-(1-methylethenyl)-,(4R,4aR,6R)-(9CI) is a chemical compound that belongs to the class of naphthalene derivatives. It is also known by its systematic name, 4R,4aR,6R-trimethyl-6-isopropenyl-1,2,3,4,4a,7-hexahydro-1-naphthalenone. This chemical is a white solid with a molecular formula of C15H22O and a molecular weight of 218.33 g/mol.
Uses
Used in Fragrance Industry:
1(2H)-Naphthalenone,3,4,4a,5,6,7-hexahydro-4,4a-dimethyl-6-(1-methylethenyl)-,(4R,4aR,6R)-(9CI) is used as a component in the production of fragrances for its unique scent and ability to enhance the overall aroma of various products.
Used in Organic Synthesis:
In the field of organic chemistry, 1(2H)-Naphthalenone,3,4,4a,5,6,7-hexahydro-4,4a-dimethyl-6-(1-methylethenyl)-,(4R,4aR,6R)-(9CI) serves as a starting material for the synthesis of various organic compounds, contributing to the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
1(2H)-Naphthalenone,3,4,4a,5,6,7-hexahydro-4,4a-dimethyl-6-(1-methylethenyl)-,(4R,4aR,6R)-(9CI) may have potential applications in the pharmaceutical industry, where it could be utilized in the development of new drugs or as an intermediate in the synthesis of existing medications. Its specific role in this industry would depend on further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 800385-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,0,3,8 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 800385-98:
(8*8)+(7*0)+(6*0)+(5*3)+(4*8)+(3*5)+(2*9)+(1*8)=152
152 % 10 = 2
So 800385-98-2 is a valid CAS Registry Number.
800385-98-2Relevant 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.