63358-20-3 Usage
Uses
Used in Pharmaceutical Industry:
(3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for selective reactions, making it an essential component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene is employed as an intermediate for the synthesis of agrochemicals. Its versatility in organic synthesis contributes to the creation of effective compounds for agricultural applications.
Used as a Protecting Group in Organic Synthesis:
The tert-butyldimethylsilyloxy group in (3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene acts as a protecting group for alcohols. This feature enables selective reactions to occur at other functional groups within the molecule, which is vital for the synthesis of complex organic molecules.
Used as a Building Block for Synthetic Transformations:
The iodo group present in (3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene makes it a valuable building block for further synthetic transformations. This attribute is beneficial in the field of organic chemistry, where the compound can be used to create a wide range of complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 63358-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,5 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63358-20:
(7*6)+(6*3)+(5*3)+(4*5)+(3*8)+(2*2)+(1*0)=123
123 % 10 = 3
So 63358-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H29IOSi/c1-7-8-9-10-13(11-12-15)16-17(5,6)14(2,3)4/h11-13H,7-10H2,1-6H3/b12-11+/t13-/m0/s1
63358-20-3Relevant academic research and scientific papers
Vik, Anders,Hansen, Trond Vidar,Kuda, Ondrej
, (2019)
Recently, several different classes of endogenous lipids have been reported that display antidiabetic and anti-inflammatory effects. Due to their minute presence in human samples, access to synthetic material of each enantiomer becomes necessary for exact structural elucidation and extensive biological evaluation. Herein we report the multi-milligram synthesis of both enantiomers of the docosahexaenoic acid ester of 13-hydroxyoctadecadienoic acid (13-DHAHLA) from commercially available starting materials.
