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8-phenyl-1-naphthalenyl boronic acid is a boronic acid derivative featuring a naphthalene ring with a phenyl group attached to it. This chemical compound is utilized in various fields, including organic synthesis, medicinal chemistry, and materials science, due to its unique structure and properties.

181135-36-4

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181135-36-4 Usage

Uses

Used in Organic Synthesis:
8-phenyl-1-naphthalenyl boronic acid is used as a building block for the synthesis of organic molecules, particularly in the formation of carbon-carbon bonds. Its ability to form stable intermediates in cross-coupling reactions makes it a valuable component in constructing complex organic structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 8-phenyl-1-naphthalenyl boronic acid is employed as a potential pharmacological agent. Its capacity to inhibit enzymes and interact with biological molecules positions it as a candidate for the development of new drugs targeting various diseases.
Used in Materials Science:
8-phenyl-1-naphthalenyl boronic acid is utilized in the development of advanced organic materials for optoelectronic devices. Its unique electronic properties and structural features contribute to the creation of materials with improved performance in areas such as solar cells, light-emitting diodes, and sensors.

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 academic research and scientific papers

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.

CHIRAL ORGANIC SANDWICH AND MULTI-LAYER CHIRALITY OF MOLECULES AND ACHIRAL DERIVATIVES

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Paragraph 0124-0125, (2020/07/08)

The present invention includes a multi-layer 3D material, a method of making, and a catalyst comprising: a first, a second, and a third layer, wherein each of the layers are arranged in a nearly parallel fashion with chirality along a center plane.

AMINE COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE INCLUDING THE SAME

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Paragraph 0193-0195, (2019/01/06)

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. An objective of the present invention is to provide an amine compound which can be used for an organic electroluminescence device having a low driving voltage, an improved lifetime and a high luminous efficiency.COPYRIGHT KIPO 2019

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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