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3-(5-BROMOPYRIDIN-3-YL)PYRIDINE, with the molecular formula C10H7BrN2, is an organic heterocyclic compound characterized by the presence of two pyridine rings, one of which is substituted with a bromine atom. This unique structure and reactivity make it a valuable compound for various applications in the fields of pharmaceuticals, agrochemicals, and materials science.

15862-22-3

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15862-22-3 Usage

Uses

Used in Pharmaceutical Industry:
3-(5-BROMOPYRIDIN-3-YL)PYRIDINE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new chemical entities with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3-(5-BROMOPYRIDIN-3-YL)PYRIDINE serves as a building block for the creation of new agrochemicals. Its reactivity and structural properties contribute to the development of innovative products for agricultural applications.
Used in Organic Materials:
3-(5-BROMOPYRIDIN-3-YL)PYRIDINE is utilized in the production of advanced organic materials. Its unique structure and reactivity make it a valuable component in the development of new materials with specific properties for various applications.
Used in Research and Development:
Due to its unique structure and reactivity, 3-(5-BROMOPYRIDIN-3-YL)PYRIDINE is of interest to researchers and chemists working in various industries. It serves as a starting material for the exploration of new chemical reactions and the development of novel compounds with potential applications in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 15862-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15862-22:
(7*1)+(6*5)+(5*8)+(4*6)+(3*2)+(2*2)+(1*2)=113
113 % 10 = 3
So 15862-22-3 is a valid CAS Registry Number.

15862-22-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-5-pyridin-3-ylpyridine

1.2 Other means of identification

Product number -
Other names 3-bromo-5-(3-pyridyl)pyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15862-22-3 SDS

15862-22-3Relevant academic research and scientific papers

Organic electroluminescent material and application thereof

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Paragraph 0028; 0030-0033, (2018/09/28)

The invention discloses an organic electroluminescent material and application thereof. The organic electroluminescent material is a compound with a structure shown as a formula I. The compound is a bipolar main body material with high efficiency and slow attenuation. Compared with almost small molecular materials recorded in the prior art, the compound m-BPySCz is slowly attenuated in a blue-light device and a green-light device under high brightness. Therefore, the organic electroluminescent material has a wide application prospect in preparation of electroluminescent devices. The formula Iis shown in the description.

Compound for preparing organic electroluminescent material

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Paragraph 0078; 0079; 0080; 0081, (2018/11/22)

The invention discloses a compound for preparing an organic electroluminescent material, and belongs to the technical field of electroluminescent materials. A synthesis method of the compound comprises the following steps that with 9-phenyl-3,6-dibromo carbazole as a raw material, a brominated carbazole group is obtained through Ullmann coupling, and reacts with n-butyllithium and trimethyl borateat minus 78 DEG C to obtain carbazole boric acid. The compound and brominated electron acceptor materials are subjected to a Suzuki coupling reaction so that the bipolar electroluminescent material containing the carbazole group can be obtained, conveying of charge carriers is regulated and balanced through double electron withdrawing groups of the main material, and therefore the quenching effect is suppressed. The compound can be used for synthesizing the main electroluminescent material. Further, the invention provides a method for synthesizing the bipolar electroluminescent material.

Substrate material for preparing bipolar electroluminescent material

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Paragraph 0046; 0078; 0079; 0080; 0081, (2019/01/07)

The invention discloses a substrate material for preparing a bipolar electroluminescent material, and belongs to the technical field of electroluminescence. A synthesis method of the substrate material comprises the steps: using 3,9'-dicarbazole as a raw material, performing Ullmann coupling to obtain brominated carbazole groups, and performing a reaction between the brominated carbazole group with n-butyllithium and trimethyl borate at -78 DEG C so as to obtain carbazole boronic acid. The bipolar electroluminescent material containing the carbazole groups can be obtained by performing a Suzuki coupling reaction between the substrate material and the brominated electron acceptor material, the adopted 3-carbazolylcarbazole has a good hole transport ability, and a high triplet energy level can be maintained by using the substrate material to synthesize the bipolar host material containing the carbazole groups, so that effective energy transfer from a host to a guest is ensured, and carrier injection and transmission ability of an electroluminescent device are improved.

Bipolar electroluminescent material comprising carbazole groups and application thereof

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Paragraph 0092-0094; 0095, (2019/01/14)

The invention relates to a preparation method and application of a bipolar electroluminescent material comprising carbazole groups, which belongs to the technical field of electroluminescence. The bipolar material adopts 3,9'-bicarbazole as an electron donating group, different n-type groups are connected on a site 2 and site 6 of the group to obtain the compound. Electron absorbing groups comprises 3-cyanopyridine, 3-diphenylphosphonyl pyridine, 5-pyrazolyl pyridine, 5-(1,2,4-triazolyl)pyridine and 3,3'-dipyridyl. According to the bipolar electroluminescent material comprising carbazole groups, the transport of a current carrier is controlled and balanced by virtue of double electron absorption groups of the main body material, so that the quenching effect can be inhibited. The bipolar electroluminescent material can be used as the main body material of a luminescent layer to be applied to an electroluminescent device.

Compounds for use in light emitting devices

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Page/Page column 44, (2016/08/03)

Optionally substituted ambipolar naphthalene compounds useful in light-emitting devices are described, including without limitation 9-(3-(10-(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)anthracen-9-yl)phenyl)-9H-carbazole and 9-(3-(10-(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)anthracen-9-yl)phenyl)-9H-carbazole.

POLYVIOLOGEN BORONIC ACID QUENCHERS FOR USE IN ANALYTE SENSORS

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Paragraph 0067; 0068, (2015/07/02)

The invention relates to a class of glucose-responsive, polyviologen boronic acid quenchers that may be used in combination with fluophores to achieve real-time measurement of glucose levels in vivo.

PYRIDINIUM BORONIC ACID QUENCHERS FOR USE IN ANALYTE SENSORS

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Page/Page column 4; 31; 40, (2009/01/20)

Novel pyridinium salts functionalized with boronic acid and methods of making them are disclosed. When combined with a fluorescent dye, the compounds are useful in the detection of polyhydroxyl-substituted organic molecules.

AMIDE DERIVATIVE

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Page/Page column 23; 24, (2008/06/13)

The present invention provides an amide derivative represented by the following general formula (1): wherein R1 represents a saturated cyclic amino group, R2 represents alkyl, halogen or haloalkyl, R3 represents hydrogen or halogen, Het 2 represents pyridyl or pyrimidinyl, and Het 1 represents a group of the formula [6], or a salt thereof, and a pharmaceutical composition comprising the same as an active ingredient. The compound of the present invention is useful as a BCR-ABL tyrosine kinase inhibitor.

2-(3-pyridyl)-carbapenem antibacterial agents

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, (2008/06/13)

Carbapenems of the formula STR1 are useful antibacterial agents.

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