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2-(4-bromo-naphthalen-1-yl)-[1,10]phenanthroline is a complex organic chemical compound characterized by a naphthalene group with a bromine atom at the 4th position, intricately linked to a phenanthroline group. The phenanthroline is further fused with a naphthalene unit, resulting in a distinctive molecular arrangement. 2-(4-bromo-naphthalen-1-yl)-[1,10]phenanthroline is recognized for its applications in organic synthesis and coordination chemistry, with its versatile structure catering to a broad spectrum of uses across scientific and industrial domains.

1853997-27-9

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1853997-27-9 Usage

Uses

Used in Organic Synthesis:
2-(4-bromo-naphthalen-1-yl)-[1,10]phenanthroline serves as a key intermediate in organic synthesis, particularly for the creation of complex organic molecules. Its unique structure allows for various chemical reactions, facilitating the synthesis of a wide array of compounds.
Used in Coordination Chemistry:
In the field of coordination chemistry, 2-(4-bromo-naphthalen-1-yl)-[1,10]phenanthroline is utilized as a ligand. Its ability to form stable complexes with metal ions makes it valuable for the development of new coordination compounds with potential applications in catalysis, materials science, and medicinal chemistry.
Used in Pharmaceutical Industry:
2-(4-bromo-naphthalen-1-yl)-[1,10]phenanthroline is employed as a building block in the design and synthesis of pharmaceutical compounds. Its structural features can be leveraged to create novel drug candidates with potential therapeutic applications.
Used in Materials Science:
2-(4-bromo-naphthalen-1-yl)-[1,10]phenanthroline is also used in materials science for the development of new materials with specific properties. Its coordination capabilities and structural attributes can contribute to the creation of materials with tailored characteristics for use in various applications, such as sensors, catalysts, or advanced materials with unique electronic or optical properties.
Used in Analytical Chemistry:
2-(4-bromo-naphthalen-1-yl)-[1,10]phenanthroline finds use in analytical chemistry as a reagent or a component in the development of assays and sensors. Its ability to interact with various analytes can be exploited for the detection and quantification of specific substances in complex samples.

Check Digit Verification of cas no

The CAS Registry Mumber 1853997-27-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,5,3,9,9 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1853997-27:
(9*1)+(8*8)+(7*5)+(6*3)+(5*9)+(4*9)+(3*7)+(2*2)+(1*7)=239
239 % 10 = 9
So 1853997-27-9 is a valid CAS Registry Number.

1853997-27-9Downstream Products

1853997-27-9Relevant academic research and scientific papers

ORGANIC COMPOUND AND ORGANIC LIGHT EMITTING DIODE AND ORGANIC LIGHT EMITTING DISPLAY DEVICE INCLUDING THE SAME

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Paragraph 109-113, (2021/03/19)

The present disclosure relates to an organic compound including a substituted or non-substituted phenanthroline moiety and a substituted or non-substituted anthracene moiety and being partially deuterated and an organic light emitting diode includes the organic compound. The organic compound has improved electron transporting property and/or the charge generation property. According, the emitting efficiency and the lifespan of the OLED and the organic light emitting display device including the organic compound in the ETL and/or the CGL are improved.

quinolone compound and organic light emitting element comprising the same

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Paragraph 0107-0109, (2019/08/26)

The present invention relates to a quinoline compound with improved efficiency, and an organic light emitting device including the same. The quinoline compound is represented by chemical formula 1. In chemical formula 1, a, b, c and d are independently an

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

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Paragraph 0400-0402; 0413-0415, (2019/02/25)

An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, wherein the organic layer comprises an emission layer and a heterocyclic compound of Formula 1: wherein a1 to a3 satisfy a1+a2+a3≥1.

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