131470-66-1 Usage
Uses
Used in Organic Chemistry:
2-(TRIBUTYLSTANNYL)-5,6-DIHYDRO-[1,4]-DIOXIN is used as a reagent for its ability to participate in various chemical reactions such as cross-coupling, cyclization, and carbon-carbon bond formation, which are essential for the synthesis of complex organic molecules.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-(TRIBUTYLSTANNYL)-5,6-DIHYDRO-[1,4]-DIOXIN is used as a precursor in the development of new drugs, contributing to the creation of molecules with potential therapeutic applications.
Used in Agrochemical Development:
2-(TRIBUTYLSTANNYL)-5,6-DIHYDRO-[1,4]-DIOXIN is utilized as a starting material in the synthesis of agrochemicals, playing a role in the production of compounds designed to enhance crop protection and yield.
Used in Materials Science:
Within the field of materials science, 2-(TRIBUTYLSTANNYL)-5,6-DIHYDRO-[1,4]-DIOXIN is employed as a component in the synthesis of advanced materials, potentially contributing to the development of new technologies and products with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 131470-66-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,4,7 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 131470-66:
(8*1)+(7*3)+(6*1)+(5*4)+(4*7)+(3*0)+(2*6)+(1*6)=101
101 % 10 = 1
So 131470-66-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H5O2.3C4H9.Sn/c1-2-6-4-3-5-1;3*1-3-4-2;/h1H,3-4H2;3*1,3-4H2,2H3;/rC16H32O2Sn/c1-4-7-12-19(13-8-5-2,14-9-6-3)16-15-17-10-11-18-16/h15H,4-14H2,1-3H3
131470-66-1Relevant articles and documents
Total Synthesis of Epicolactone
Kravina, Alberto G.,Carreira, Erick M.
supporting information, p. 13159 - 13162 (2018/09/21)
The biologically active and structurally complex secondary metabolite epicolactone is a member of the natural product pool found in cash crop endophytes of the genus Epicoccum. By exploiting inherent reactivity, a total synthesis of this highly oxygenated