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4-CHLORO-2,6-DIPHENYLPYRIMIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29509-91-9

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29509-91-9 Usage

Chemical Properties

White solid

Synthesis Reference(s)

Journal of Medicinal Chemistry, 47, p. 6529, 2004 DOI: 10.1021/jm049448r

Check Digit Verification of cas no

The CAS Registry Mumber 29509-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,0 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29509-91:
(7*2)+(6*9)+(5*5)+(4*0)+(3*9)+(2*9)+(1*1)=139
139 % 10 = 9
So 29509-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H11ClN2/c17-15-11-14(12-7-3-1-4-8-12)18-16(19-15)13-9-5-2-6-10-13/h1-11H

29509-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2,6-diphenylpyrimidine

1.2 Other means of identification

Product number -
Other names 2,6-Diphenyl-4-chlorpyrimidin

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:29509-91-9 SDS

29509-91-9Relevant academic research and scientific papers

Aromatic compound and organoelectroluminescent device comprising the compound

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Paragraph 0519; 0571-0576, (2021/08/31)

The present invention relates to an aromatic compound and an organic electroluminescent device including the same. The aromatic compound is represented by chemical formula 1, and the organic electroluminescent device is excellent in driving voltage, luminous efficiency and lifetime characteristics.

Compound, high polymer, mixture, composition and organic electronic device

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Paragraph 0251-0256, (2020/11/12)

The invention discloses a compound, a high polymer, a mixture, a composition and an organic electronic device. The compound is shown as a general formula (1), a triphenylene fused ring and a nitrogen-containing heterocyclic ring unit are respectively connected to an ortho-group-containing substituted aromatic ring to help molecular dispersion of the compound to reduce quenching of excitons, so that the device performance and stability of the compound are improved, and an effective scheme is provided for improving the performance and prolonging the service life of organic electronic devices, especially OLEDs.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING SAME, AND ELECTRONIC DEVICE COMPRISING SAME

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Paragraph 0253; 0254, (2018/09/23)

The present invention provides a novel compound capable of improving the light emitting efficiency, stability and life span of a device, and an organic electric element and an electronic device using the same.

COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT COMPRISING THE SAME AND ELECTRONIC DEVICE THEREOF

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Paragraph 0222; 0223, (2018/10/21)

The present invention provides the compound represented by Formula 1, and an organic electric element comprising a first electrode, a second electrode, and an organic material layer formed between the first electrode and the second electrode, wherein the organic material layer comprises the compound represented by Formula 1. The driving voltage of an organic electronic device can be lowered, and the luminous efficiency, color purity and life time of an organic electronic device can be improved by comprising the compound represented by Formula 1 in the organic material layer.

COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT COMPRISING THE SAME AND ELECTRONIC DEVICE THEREOF

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Paragraph 0400-0402, (2018/02/03)

The present invention provides: a compound having high light-emitting efficiency, having low driving voltage, and improving the lifespan of a device; an organic electric element using the same; and an electronic device thereof. The compound is represented by chemical formula 1. In the chemical formula 1, X is one of N-L^1-R^1 S, O, CR^aR^b; n and m are 0 or 1, and n+m is at least 1 (here, when n is 0, A is a single bond, and when m is 0, B is a single bond); A and B are independently one of a single bond, N-L^2-R^2, S, O, CR^cR^d; and Z^1 to Z^12 are independently CR^3, N, wherein at least one is N, and each CR^3 is independently the same or different when at least two of Z^1 to Z^12 are CR^3.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transporting layer(141) Buffer layer(150) Light-emitting layer(151) Light-emitting assisting layer(160) Electron transfer layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2017

COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT COMPRISING THE SAME AND ELECTRONIC DEVICE THEREOF

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Paragraph 0511; 0512, (2018/02/03)

The present invention refers to for high luminous efficiency, compounds capable of low driving voltage on the organic layer, the organic electric element and electronic device using the same number [...] substrate. (by machine translation)

NOVEL PYRIMIDINE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND COMPOSITIONS CONTAINING THEM

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Page/Page column 257, (2008/06/13)

The present invention provides new heterocyclic compounds, particularly substituted pyrimidines, methods and compositions for making and using these heterocyclic compounds, and methods for treating a variety of diseases and disease states, including atherosclerosis, arthritis, restenosis, diabetic nephropathy, or dyslipidemia, or disease states mediated by the low expression of Perlecan.

SUBSTITUTED PYRIMIDINES AS LIGANDS OF ADENOSINE RECEPTORS

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Page/Page column 25, (2008/06/13)

The invention provides a compound of formula (I) wherein R and R' are selected from hydrogen, alkyl, alkenyl, alkynyl, or aryl; R'' and R''' are selected from hydrogen, acyl, thio-acyl, seleno-acyl, alkyl, alkenyl, alkynyl, or aryl; or a pharmaceutically

2,4,6-Trisubstituted pyrimidines as a new class of selective adenosine A1 receptor antagonists

Chang, Lisa C. W.,Spanjersberg, Ronald F.,Von Frijtag Drabbe Künzel, Jacobien K.,Mulder-Krieger, Thea,Van Den Hout, Gijs,Beukers, Margot W.,Brussee, Johannes,IJzerman, Adriaan P.

, p. 6529 - 6540 (2007/10/03)

Adenosine receptor antagonists usually possess a bi- or tricyclic heteroaromatic structure at their core with varying substitution patterns to achieve selectivity and/or greater affinity. Taking into account molecular modeling results from a series of pot

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