30169-71-2 Usage
Uses
Used in Organic Synthesis:
2-BUTYL-1,3,2-DIOXABORINANE is used as a reagent for the formation of carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction. This reaction is a powerful tool in organic synthesis, allowing for the creation of new chemical entities with potential applications across various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-BUTYL-1,3,2-DIOXABORINANE is utilized in the preparation of various drugs. Its role in facilitating carbon-carbon bond formation is crucial for the synthesis of complex molecular structures that can exhibit therapeutic effects.
Used in Agrochemical Industry:
2-BUTYL-1,3,2-DIOXABORINANE is also employed in the development of agrochemicals. Its ability to form carbon-carbon bonds aids in the synthesis of compounds that can be used in pesticides, herbicides, and other agricultural applications to improve crop yields and protect plants from pests.
Used in Electronic Materials:
Furthermore, 2-BUTYL-1,3,2-DIOXABORINANE finds application in the creation of materials for electronic applications. Its role in bond formation contributes to the development of advanced materials used in electronic devices and components, enhancing their performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 30169-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30169-71:
(7*3)+(6*0)+(5*1)+(4*6)+(3*9)+(2*7)+(1*1)=92
92 % 10 = 2
So 30169-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H15BO2/c1-2-3-5-8-9-6-4-7-10-8/h2-7H2,1H3
30169-71-2Relevant academic research and scientific papers
Production of optically pure organoboranes
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, (2008/06/13)
A process for upgrading to essentially 100% enantiomeric excess the optical purity of an organoborane intermediate represented by the formulae: or wherein Icp is isopinocampheyl and R* is a unsubstituted or substituted, acyclic or cyclic alkyl having from 4 to 30 carbon atoms, comprising the steps of hydroborating cis-alkene, a trans-alkene or a tertiary-alkene with monoisopinocampheylborane or diisopinocampheylborane, obtaining a solid organoborane and recrystallizing the solid organoborane to obtain an enantiomeric excess of essentially 100% ee of said organoborane.
