769140-74-1 Usage
General Description
13-Methyl-8,11,13-podocarpatriene-3,12-diol is a complex chemical compound belonging to the podocarpatriene family. It is a diterpene alcohol, which means it is derived from the terpene hydrocarbon. 13-Methyl-8,11,13-podocarpatriene-3,12-diol is known for its potential biological activities, particularly in the field of medicinal research. It has shown anti-inflammatory and anti-cancer properties, making it a potential candidate for drug development. The structure of 13-Methyl-8,11,13-podocarpatriene-3,12-diol also suggests potential applications in the fragrance and flavor industry due to its aromatic characteristics. Overall, this compound holds promise for various industrial and pharmaceutical applications due to its unique chemical structure and potential bioactivities.
Check Digit Verification of cas no
The CAS Registry Mumber 769140-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,9,1,4 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 769140-74:
(8*7)+(7*6)+(6*9)+(5*1)+(4*4)+(3*0)+(2*7)+(1*4)=191
191 % 10 = 1
So 769140-74-1 is a valid CAS Registry Number.
769140-74-1Relevant articles and documents
Palladium-Catalyzed α-Arylation of Cyclic Vinylogous Esters for the Synthesis of γ-Arylcyclohexenones and Total Synthesis of Aromatic Podocarpane Diterpenoids
Hou, Wen-Yi,Wu, Yen-Ku
, p. 1220 - 1223 (2017)
Described is a method for the formal γ-arylation of cyclohexenones allowing synthesis of a remote all-carbon quaternary center. The process involves the palladium-catalyzed α-arylation of a α-substituted cyclic vinylogous ester followed by the Stork-Danheiser transposition. The synthetic utility of this protocol is featured in the total syntheses of (±)-12-hydroxy-13-methylpodocarpa-8,11,13-trien-3-one, (±)-3β,12-dihydroxy-13-methylpodocarpane-8,11,13-triene, and (±)-O-methyl nimbinone.
