5202-25-5 Usage
Description
(1R,2S,5E,9Z)-5,9-Cyclododecadien-1,2-diol, also known as Cyclododecadienol, is a naturally occurring organic compound commonly found in plants. It is a bicyclic diol with a double bond at position 5 and a conjugated diene system.
Used in Fragrance Industry:
(1R,2S,5E,9Z)-5,9-Cyclododecadien-1,2-diol is used as a fragrance ingredient for its pleasant, floral odor in various cosmetics and personal care products.
Used in Pharmaceutical Industry:
(1R,2S,5E,9Z)-5,9-Cyclododecadien-1,2-diol has potential applications as a pharmaceutical compound due to its unique structure and properties.
Used in Agrochemical Industry:
(1R,2S,5E,9Z)-5,9-Cyclododecadien-1,2-diol also has potential applications in the agrochemical industry, although the specific uses are not detailed in the provided materials.
Check Digit Verification of cas no
The CAS Registry Mumber 5202-25-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5202-25:
(6*5)+(5*2)+(4*0)+(3*2)+(2*2)+(1*5)=55
55 % 10 = 5
So 5202-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c13-11-9-7-5-3-1-2-4-6-8-10-12(11)14/h3-6,11-14H,1-2,7-10H2/b5-3+,6-4+
5202-25-5Relevant articles and documents
Concise syntheses of the natural products (+)-sylvaticin and (+)-cis-sylvaticin
Donohoe, Timothy J.,Harris, Robert M.,Williams, Oliver,Hargaden, Grainne C.,Burrows, Jeremy,Parker, Jeremy
scheme or table, p. 12854 - 12861 (2010/01/29)
Two concise syntheses of the natural products cis-sylvaticin and sylvaticin are reported, using oxidative cyclization methodology as the key step. A sequential solvolysis/hydride shift/intramolecular reduction cascade was used to establish the trans stereochemistry of one of the THF rings of sylvaticin.
Selective Asymmetric Dihyroxylation of Polyenes
Becker, Heinrich,Soler, Marcos A.,Sharpless, K. Barry
, p. 1345 - 1376 (2007/10/02)
The asymmetric dihydroxylation procedure (AD) is applied to a variety of polyenes.In many cases excellent regioselectivities are obtained.The observed selectivities are rationalized in terms of electronic and/or steric inherent to the substrate, superimposed on the substrate's favorable or unfavorable interactions with the binding pocket of the AD ligand.Surprisingly, for medium and large ring olefins with trans-double bonds outstanding enantioselectivities are realized using the pyrimidine ligands.A hexaol of D3 symmetry is prepared from all trans cyclodecatriene.