102616-14-8 Usage
Description
(4E)-2-(benzyloxy)-3,7-dimethyl-1-[(1E)-prop-1-en-1-yl]oct-4-en-1-yl (benzyloxy)acetate is a complex organic compound characterized by a long molecular structure with multiple functional groups, including benzyloxy and acetate, as well as double bonds and methyl groups. This synthetic or semi-synthetic derivative is likely to be of interest in the pharmaceutical or chemical industry due to its specific properties and potential for diverse applications.
Used in Pharmaceutical Industry:
(4E)-2-(benzyloxy)-3,7-dimethyl-1-[(1E)-prop-1-en-1-yl]oct-4-en-1-yl (benzyloxy)acetate is used as a pharmaceutical compound for its potential therapeutic applications. Its complex structure and multiple functional groups may contribute to its interaction with biological targets, making it a candidate for further research and development in drug discovery.
Used in Chemical Industry:
In the chemical industry, (4E)-2-(benzyloxy)-3,7-dimethyl-1-[(1E)-prop-1-en-1-yl]oct-4-en-1-yl (benzyloxy)acetate is used as a chemical intermediate or building block for the synthesis of other complex organic molecules. Its diverse functional groups and structural features make it a valuable component in the creation of new materials or compounds with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 102616-14-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,1 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102616-14:
(8*1)+(7*0)+(6*2)+(5*6)+(4*1)+(3*6)+(2*1)+(1*4)=78
78 % 10 = 8
So 102616-14-8 is a valid CAS Registry Number.
102616-14-8Relevant articles and documents
Stereocontrolled Synthesis of Highly Oxygenated Acyclic Systems via the Enolate Claisen Rearrangement of O-Protected Allylic Glycolates
Gould, Thomas J.,Balestra, Michael,Wittman, Mark D.,Gary, Jill A.,Rossano, Lucius T.,Kallmerten, James
, p. 3889 - 3901 (2007/10/02)
Enolate Claisen rearrangement of E- and Z-allylic glycolates yields the syn- and anti-2-alkoxy-3-alkyl 4-enoates, respectively, in good yields (60-90percent) and with high internal diastereoselectivity.Incorporation of the glycolate Claisen procedure into an iterative sequence consisting of Claisen rearrangement and homologation by addition of vinyl nucleophiles results in the efficient, stereocontrolled generation of remotely functionalized, highly oxygenated acyclic systems.This strategy is demonstrated in stereoselective syntheses of pine sawfly pheromone 42 and tocopherol side-chain intermediate 30.
