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5-bromo-4-methyl-2-phenylPyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31686-64-3

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31686-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31686-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31686-64:
(7*3)+(6*1)+(5*6)+(4*8)+(3*6)+(2*6)+(1*4)=123
123 % 10 = 3
So 31686-64-3 is a valid CAS Registry Number.

31686-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-4-methyl-2-phenylpyridine

1.2 Other means of identification

Product number -
Other names 5-BROMO-4-METHYL-2-PHENYL-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:31686-64-3 SDS

31686-64-3Relevant academic research and scientific papers

NAPHTHYRIDINES AS INHIBITORS OF HPK1

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Paragraph 2238; 2239, (2018/10/21)

Naphthyridine compounds and their use as inhibitors of HPK1 are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the naphthyridine compounds.

N - aryl - hydrogel arc [tin [tin] light-emitting electroluminescent device as a component of

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Paragraph 0131-0132, (2018/05/15)

wherein Ar is C3-C25 aryl in which at least one aromatic ring atom is nitrogen; X is O, S or CR9R10; R1, R2, R3, R4, R5 and R6 independently are hydrogen, deuterium, C1-C12 alkyl, C4-C12 aryl or C2-C12 alkenyl; R7 and R8 independently are hydrogen, deuterium, C1-C12 alkyl, C4-C12 aryl or C2-C12 alkenyl or R7 and R8 groups attached to a nitrogen atom are joined by a single bond, O, S or CR11R12 to form a single nitrogen-containing substituent; R9 and R10 independently are hydrogen, deuterium, C1-C12 alkyl, C4-C12 aryl or C2-C12 alkenyl; and R11 and R12 independently are hydrogen, deuterium, C1-C12 alkyl, C4-C12 aryl or C2-C12 alkenyl; provided that Ar does not contain an aromatic ring attached to the tricyclic nucleus which contains more than two aromatic ring nitrogen atoms.

LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE

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Paragraph 0389-0390, (2017/10/26)

A novel organometallic complex with high reliability is provided. A light-emitting element includes an EL layer between a pair of electrodes. The EL layer includes at least a light-emitting layer. The light-emitting layer contains an organometallic complex. The organometallic complex includes a first ligand and a second ligand which are coordinated to a central metal. The HOMO is distributed over the first ligand, and the LUMO is distributed over the second ligand. The first ligand and the second ligand are cyclometalated ligands.

ORGANOMETALLIC COMPLEX, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE

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Paragraph 0330; 0331; 0332, (2017/10/31)

To provide a novel organometallic complex. The organometallic complex is represented by Formula (G1) and includes a central metal, a first ligand, and a second ligand. The first ligand and the second ligand are cyclometalated ligands. At least one of the

ORGANOMETALLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

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Paragraph 0351, (2016/07/27)

An organometallic compound represented by Formula 1: [in-line-formulae]M(L1)n1(L2)n2??Formula 1[/in-line-formulae]wherein in Formula 1, M, L1, L2, n1, and n2 are the same as described in th

Organometallic compound and organic light emitting device including the same

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Paragraph 0379-0382, (2016/10/09)

Disclosed are an organometallic compound and an organic light-emitting device comprising the organometallic compound. The organometallic compound is represented by chemical formula 1. The organometallic compound has excellent electrical properties and thermal stability. The organic light-emitting device comprising the organometallic compound can have a low driving voltage, high efficiency, long lifespan, and excellent color purity.COPYRIGHT KIPO 2016

Organometallic compound, organic light-emitting device including same and method of manufacturing organic light-emitting device

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Paragraph 0354; 0355; 0356; 0357, (2016/10/10)

The invention relates to an organometallic compound, an organic light-emitting device including the same and a method of manufacturing the organic light-emitting device. The organometallic compound represented by Formula 1, wherein M is selected from iridium (Ir), platinum (Pt), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf), europium (Eu), terbium (Tb), thulium (Tm), and rhodium (Rh), and wherein L 1 is a ligand represented by Formula 2A and L 2 is a ligand represented by Formula 2B, and wherein L 1 and L 2 in Formula 1 are different from each other.

ORGANOMETALLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

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Paragraph 0421; 0422, (2016/10/04)

An organometallic compound represented by Formula 1: [in-line-formulae]M(L1)n1(L2)n2??Formula 1[/in-line-formulae] wherein in Formulae 1, 2A, and 2B, groups and substituents are the same as disclosed in the specification.

Organic electroluminescent device employing organic light emitting compound as light emitting material

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Paragraph 0033; 0050, (2015/04/15)

Provided is an organic electroluminescent device that exhibits an efficient host-dopant energy transfer mechanism, and thus, expresses a certain high-efficiency electroluminescent performance, based on improved electron density distribution. The organic electroluminescent device also overcomes low initial efficiency and short operation life property, and secures high-performance electroluminescent performance with high efficiency and long life property for each color.

Diarylamino Substituted Metal Complexes

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Paragraph 0116-0118, (2014/02/16)

Heteroleptic complexes having at least one diarylamino or carbazole group, as shown in Formula (I), are provided: wherein R1, R2, R3, R4, R5, and R6 each represent mono, di, tri, tetra, or penta substitutions or no substitution; wherein Z is a single bond connecting the two phenyl rings, or is absent, wherein when Z is absent, the positions on the phenyl rings may be substituted by R5 or R6; wherein any two adjacent substituents are optionally joined together to form a ring, which may be further substituted; wherein each of R1, R2, R3, R4, R5, and R6 is independently selected from various substituents; and wherein m is 1 or 2. Devices, such as organic light emitting devices (OLEDs) that comprise phosphorescent light emitting materials are also provided.

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