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2-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)but-3-enyloxy]tetrahydropyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

313342-78-8

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313342-78-8 Usage

Molecular Structure

Consists of a tetrahydropyran ring with attached but-3-enyloxy and dioxaborolane groups.

Dioxaborolane Group

Contains boron and oxygen atoms; commonly used as a protecting group in organic synthesis.

But-3-enyloxy Group

A functional group frequently found in organic compounds.

Potential Applications

Interest in organic synthesis, potential applications in medicinal chemistry or material science.

Further Research

Precise properties and potential uses require additional research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 313342-78-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,3,4 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 313342-78:
(8*3)+(7*1)+(6*3)+(5*3)+(4*4)+(3*2)+(2*7)+(1*8)=108
108 % 10 = 8
So 313342-78-8 is a valid CAS Registry Number.

313342-78-8Downstream Products

313342-78-8Relevant academic research and scientific papers

Stereoselective synthesis of (E)-vinylboronic esters via a Zr mediated hydroboration of alkynes

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Page/Page column 4, (2008/06/13)

There is herein provided a process for Zr-mediated hydroboration of alkynes which offers (E)-vinylboronic esters in high yield with stereoselectivity and regioselectivity.

Zr-Mediated hydroboration: Stereoselective synthesis of vinyl boronic esters

Wang, Yanong D.,Kimball, Gregory,Prashad, Amar S.,Wang, Yan

, p. 8777 - 8780 (2007/10/03)

An improved process for the preparation of (E)-vinylboronic esters via a Zr-mediated hydroboration of alkynes, especially oxygen-containing alkynes, is described.

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