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181135-36-4

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181135-36-4 Usage

General Description

8-phenyl-1-naphthalenyl boronic acid is a chemical compound used in organic synthesis and medicinal chemistry. It is a boronic acid derivative that contains a naphthalene ring with a phenyl group attached to it. 8-phenyl-1-naphthalenyl boronic acid is commonly used as a building block in the synthesis of organic molecules, particularly in the formation of carbon-carbon bonds. It has also been investigated for its potential pharmacological properties, including its ability to inhibit enzymes and interact with biological molecules. Additionally, 8-phenyl-1-naphthalenyl boronic acid has been studied for its potential use in materials science, particularly in the development of advanced organic materials for optoelectronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 181135-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,1,3 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 181135-36:
(8*1)+(7*8)+(6*1)+(5*1)+(4*3)+(3*5)+(2*3)+(1*6)=114
114 % 10 = 4
So 181135-36-4 is a valid CAS Registry Number.

181135-36-4Downstream Products

181135-36-4Relevant articles and documents

Compound and application thereof

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Paragraph 0094-0095; 0097, (2021/06/22)

The invention relates to a compound and application thereof. The compound has a structure as shown in a formula I. By introducing a carbazole structure of cycloheptatriene, the planarity of molecules is improved, and the transmission barrier of current carriers is reduced, so that an organic electroluminescent device comprising the compound has the advantages of low voltage and high efficiency.

AMINE COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE INCLUDING THE SAME

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, (2018/06/20)

The present invention relates to an amine compound and an organic electroluminescence device including the same. The amine compound according to one embodiment of the present invention is represented by chemical formula 1. In chemical formula 1, Ar1 and Ar2 each independently represent a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted phenanthryl group A substituted or unsubstituted fluorenyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group.COPYRIGHT KIPO 2018

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