104113-52-2 Usage
General Description
The chemical compound "(5S,6S,9S,10R,15R)-19,20-dioxo-5,6,7,8,9,10,11,14-octahydro-5,10:9,15-dicycloretinol" is a complex molecule with a long and intricate name. It is a cycloretinoid derivative, meaning it is derived from a cyclic form of a retinoid compound. (5S,6S,9S,10R,15R)-19,20-dioxo-5,6,7,8,9,10,11,14-octahydro-5,10:9,15-dicycloretinol has a molecular structure with multiple ring formations and two ketone functional groups. It has a total of 20 carbon atoms and is highly oxygenated. It may have potential applications in pharmacology or medical research due to its unique structure and potentially valuable biological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 104113-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,1 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104113-52:
(8*1)+(7*0)+(6*4)+(5*1)+(4*1)+(3*3)+(2*5)+(1*2)=62
62 % 10 = 2
So 104113-52-2 is a valid CAS Registry Number.
104113-52-2Relevant articles and documents
Total Synthesis of the Labdane Diterpenes Galanal A and B from Geraniol
Lin, Shih-Che,Chein, Rong-Jie
, p. 1575 - 1583 (2017/02/10)
The first total synthesis of galanal A and B has been achieved from naturally occurring geraniol. Key steps in this synthesis are the use of a Lewis acid assisted chiral Br?nsted acid (chiral LBA) mediated cationic polyene cyclization and a titanocene-mediated radical cyclization for the asymmetric assembly of the "AB" ring and the construction of the all-carbon quaternary center at the junction of the "BC" ring, respectively.
Synthesis of labdane diterpenes galanal A and B from (+)-sclareolide
Kumar, Chebolu Naga Sesha Sai Pavan,Chein, Rong-Jie
supporting information, p. 2990 - 2992 (2014/06/23)
The first chemical synthesis of galanal A and B was achieved by a concise and highly efficient pathway starting from commercially available (+)-sclareolide and features a Wittig reaction and a titanocene-mediated radical cyclization as the key steps.
