58322-11-5 Usage
Description
(1R,3aR,7aR)-1-((2R,5S)-5,6-dimethylheptan-2-yl)-7a-methylhexahydro-1H-inden-4(2H)-one is a complex ketone derivative featuring a hexahydro-1H-inden ring system with a 2-heptyl group and a methyl group at specific positions. This chiral compound has a chemical formula of C19H34O and exists as a colorless liquid at room temperature. Its properties and applications are contingent upon its synthesis and intended use.
Uses
Used in Pharmaceutical Industry:
(1R,3aR,7aR)-1-((2R,5S)-5,6-dimethylheptan-2-yl)-7a-methylhexahydro-1H-inden-4(2H)-one is used as a pharmaceutical intermediate for the development of novel drugs due to its unique molecular structure and chiral centers, which may offer specific biological activities and therapeutic benefits.
Used in Chemical Synthesis:
In the field of organic chemistry, this compound serves as a key intermediate in the synthesis of more complex organic molecules, potentially leading to advancements in material science and the creation of new chemical entities with various applications.
Used in Research and Development:
(1R,3aR,7aR)-1-((2R,5S)-5,6-dimethylheptan-2-yl)-7a-methylhexahydro-1H-inden-4(2H)-one is utilized in academic and industrial research settings to study its chemical properties, reactivity, and potential interactions with other molecules, which can contribute to the discovery of new chemical processes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 58322-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,2 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58322-11:
(7*5)+(6*8)+(5*3)+(4*2)+(3*2)+(2*1)+(1*1)=115
115 % 10 = 5
So 58322-11-5 is a valid CAS Registry Number.
58322-11-5Relevant articles and documents
Synthesis of two osteoclast-forming suppressors, demethylincisterol A 3 and chaxine A
Yajima, Arata,Kagohara, Yuuma,Shikai, Keisuke,Katsuta, Ryo,Nukada, Tomoo
, p. 1729 - 1735 (2012/03/10)
The synthesis of two potent osteoclast-forming suppressing agents isolated from the Chinese mushroom Agrocybe chaxingu, demethylincisterol A3 and chaxine A, was accomplished using ergocalciferol as the starting material. Our methodology for the synthesis of demethylincisterol A3 and chaxine A featured the construction of a butenolide moiety by the intramolecular Horner-Wadsworth-Emmons reaction under Masamune-Roush conditions. This is the first reported synthesis of chaxine A.
On the Julia Alkenylation reaction in vitamin D synthesis. Isolation of four geometrical isomers of vitamin D4
Blakmore,Grzywacz,Kocienski,Marczak,Wicha
, p. 1209 - 1217 (2007/10/03)
Coupling of sulfone 2 and aldehyde 3b using the Julia alkenylation procedure has been reexamined using modern product separation techniques. It was found that vitamin D4 1b and its geometric isomers 10, 11 and 12 are formed in a ratio of 75:10:10:5, respectively. The building blocks 2 and 3b were prepared from vitamin D2. Correlations for the structure assignment of vitamin D stereoisomers by 1H NMR spectroscopy are presented.
