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1-phenyloctane-3,3-diboronic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78782-34-0

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78782-34-0 Usage

Molecular structure

A phenyl group attached to an octane backbone with two boronic acid functional groups.

Functional groups

Two boronic acid functional groups.

Potential applications

Synthesis of complex molecules in organic chemistry.

Reactivity

Ability to form stable complexes with diols and used in the Suzuki-Miyaura cross-coupling reaction to create carbon-carbon bonds.

Further functionalization

Presence of the phenyl group provides opportunities for further functionalization and diversification of the molecule for various applications in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 78782-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,8 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78782-34:
(7*7)+(6*8)+(5*7)+(4*8)+(3*2)+(2*3)+(1*4)=180
180 % 10 = 0
So 78782-34-0 is a valid CAS Registry Number.

78782-34-0Downstream Products

78782-34-0Relevant academic research and scientific papers

Deprotonation of 1,1-diboronic esters and reactions of the carbanions with alkyl halides and carbonyl compounds

Matteson, Donald S.,Moody, Robert J.

, p. 20 - 28 (2008/10/08)

The efficient deprotonation of 1,1-diboronic esters has been accomplished with lithium 2,2,6,6-tetramethylpiperidide in the presence of tetramethylethylenediamine in tetrahydrofuran. Bis(l,3,2-dioxaborin-2-yl)methane, (C3H6O2/s

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