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63358-20-3

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63358-20-3 Usage

General Description

"(3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene" is a chemical compound with a molecular formula of C12H25IOSi. It is a chiral compound, with a stereocenter at the third carbon atom. (3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene is commonly used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. The tert-butyldimethylsilyloxy group is a protecting group for alcohols, which allows for selective reactions to take place at other functional groups in the molecule. The iodo group also makes this compound a valuable building block for further synthetic transformations. Overall, this compound has diverse applications in the field of organic chemistry and is an important tool for the creation 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

63358-20-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:63358-20-3 SDS

63358-20-3Downstream Products

63358-20-3Relevant articles and documents

Synthesis of both enantiomers of the docosahexaenoic acid ester of 13-hydroxyoctadecadienoic acid (13-DHAHLA)

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.

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