79379-67-2 Usage
Molecular Weight
268.31 g/mol The molecular weight of the compound is 268.31 g/mol, calculated based on the atomic weights of carbon, hydrogen, and oxygen.
Indenes
Polycyclic Aromatic Compounds Indenes are a class of polycyclic aromatic compounds that contain a six-membered ring fused to a benzene ring. This compound belongs to this class of compounds.
Ethyl Ester Derivative
1H-Indene-1-carboxylic Acid The compound is an ethyl ester derivative of 1H-Indene-1-carboxylic acid, which means that an ethoxy group (-OCH2CH3) has been added to the carboxylic acid functional group of the parent compound.
Potential Pharmacological Properties
Anti-inflammatory and Analgesic The compound has potential pharmacological properties as an anti-inflammatory and analgesic agent, making it a valuable target for further research and development in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 79379-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,7 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79379-67:
(7*7)+(6*9)+(5*3)+(4*7)+(3*9)+(2*6)+(1*7)=192
192 % 10 = 2
So 79379-67-2 is a valid CAS Registry Number.
79379-67-2Relevant articles and documents
Rhodium-catalyzed carbonylation of alkynes in the presence of alcohols: Selective synthesis of 3-alkoxycarbonylindanones
Yoneda, Eiji,Kaneko, Takayuki,Zhang, Shi-Wei,Onitsuka, Kiyotaka,Takahashi, Shigetoshi
, p. 7811 - 7814 (2007/10/03)
Rhodium-catalyzed cyclic carbonylation of alkynes 1 in the presence of alcohols gives selectively 3-alkoxycarbonylindanones 2 which are derived from 1, one molecule of alcohol and two molecules of carbon monoxide.
RHODIUM CARBONYL-CATALYZED CARBONYLATION OF ACETYLENES IN THE PRESENCE OF OLEFINS AND PROTON DONORS. SYNTHESIS OF 5-ALKYL-2(5H)-FURANONES.
Hong, Pangbu,Mise, Takaya,Yamazaki, Hiroshi
, p. 989 - 992 (2007/10/02)
Rhodium carbonyl-catalyzed reactions of internal acetylenes with ethylene and CO in protic solvents, e.g., ethanol, gave 3,4-disubstituted-5-ethyl-2(5H)-furanones in good yields.By using propylene or methyl acrylate instead of ethylene, small amounts of 5-n-/isopropyl-2(5)H-furanones or 5--2(5H)-furanone were obtained.
