59909-34-1 Usage
Description
(1R,4aR,4bS,10aR)-Methyl 2,4b,8,8,10a-pentamethyl-1,4,4a,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylate is a synthetic chemical compound belonging to the phenanthrene family. It features a complex fused-ring structure and is characterized by its molecular formula C26H44O2. As a carboxylate ester derivative of pentamethyl-1,4,4a,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid, this compound is primarily utilized in the realm of organic chemistry for research and exploration purposes. Its intricate and specific molecular architecture suggests potential applications in pharmaceutical and medicinal chemistry, although it is not commonly found in commercial or industrial settings due to its specialized nature.
Uses
Used in Organic Chemistry Research:
(1R,4aR,4bS,10aR)-Methyl 2,4b,8,8,10a-pentamethyl-1,4,4a,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylate serves as a valuable compound in organic chemistry research. Its unique structure allows scientists to investigate various chemical reactions and mechanisms, contributing to the advancement of knowledge in this scientific field.
Used in Pharmaceutical and Medicinal Chemistry:
While not widely commercialized, the compound holds promise for applications in pharmaceutical and medicinal chemistry. Its complex structure may offer novel properties that could be harnessed in the development of new drugs or therapeutic agents, making it a subject of interest for researchers in these domains.
Check Digit Verification of cas no
The CAS Registry Mumber 59909-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,0 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59909-34:
(7*5)+(6*9)+(5*9)+(4*0)+(3*9)+(2*3)+(1*4)=171
171 % 10 = 1
So 59909-34-1 is a valid CAS Registry Number.
59909-34-1Relevant articles and documents
The first biomimetic synthesis of a diterpenoid with the ent-verrucosin A/B skeleton
Grinco, Marina,G?rbu, Vladilena,Gorincioi, Elena,Barba, Alic,Kulci?ki, Veaceslav,Ungur, Nicon
, p. 2084 - 2086 (2016)
The first biomimetic synthesis of methyl (8S,9R,13R,14R)-4,4,8,9,13-pentamethyl-20(10 → 9)-abeo-ent-isocopal-5(10),11(12)-dien-15-oate - a diterpenoid with the ent-verrucosin A/B skeleton has been performed by electrophilic isomerization of methyl 12α-hydroxy-ent-isocopal-13(16)-en-15-oate. The structure and stereochemistry of the synthesized compound have been established on the basis of spectroscopic data.
CYCLIZATION AND REARRANGEMENTS OF DITERPENOIDS X. SUPERACID CYCLIZATION OF LABD-8,13E- AND -8,13Z-DIEN-15-OIC ACIDS AND THEIR ESTERS
Ungur, N. D.,Tuen, Nguen Van,Vlad, P. F.
, p. 642 - 643 (1991)
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CYCLIZATION AND REARRANGEMENTS OF DITERPENOIDS X. SUPERACID CYCLIZATION OF E,E,E- AND Z,E,E-GERANYLGERANIC ACIDS AND THEIR ESTERS
Ungur, N. D.,Tuen, Nguen Van,Vlad, P. F.
, p. 644 (2007/10/02)
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