15786-26-2 Usage
Description
(1Z,3E)-cyclododeca-1,3-diene-1,2-diol is a dihydroxy compound with a cyclic structure, featuring two hydroxyl groups and two double bonds within its molecular structure. This diene diol is known for its unique chemical and physical properties, making it a promising candidate for various applications across different industries.
Uses
Used in Polymer and Resin Production:
(1Z,3E)-cyclododeca-1,3-diene-1,2-diol is used as a monomer in the production of polymers and resins, contributing to the development of materials with specific properties tailored for various applications.
Used in Organic Synthesis:
(1Z,3E)-cyclododeca-1,3-diene-1,2-diol serves as a key intermediate in the synthesis of various organic compounds, enabling the creation of a wide range of chemical products.
Used in Pharmaceutical and Medicinal Applications:
(1Z,3E)-cyclododeca-1,3-diene-1,2-diol is used as a starting material or intermediate in the development of pharmaceuticals and medicines, potentially leading to new treatments and therapies.
Used in Research and Development:
Due to its unique structure and properties, (1Z,3E)-cyclododeca-1,3-diene-1,2-diol is utilized in research and development efforts across various industries, driving innovation and the discovery of new applications.
Check Digit Verification of cas no
The CAS Registry Mumber 15786-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,8 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15786-26:
(7*1)+(6*5)+(5*7)+(4*8)+(3*6)+(2*2)+(1*6)=132
132 % 10 = 2
So 15786-26-2 is a valid CAS Registry Number.
15786-26-2Relevant 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.
