182918-13-4

Basic information

• Product Name: 2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine
• Synonyms: 2-chloro-4,6-di(biphenyl-4-yl)-1,3,5-triazine;1,3,5-Triazine, 2,4-bis([1,1'-biphenyl]-4-yl)-6-chloro-;2,4-Bis(4-biphenylyl)-6-chloro-1,3,5-triazine;2,4-Di([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine;2-chloro-4,6-bis(4-biphenylyl)-1,3,5-triazine;2,4-Bis-biphenyl-4-yl-6-chloro-[1,3,5]triazine;2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine;2,4-di(biphenyl-4-yl)-6-chloro-1,3,5-triazine
• CAS NO: 182918-13-4
• Molecular Formula: C27H18ClN3
• Molecular Weight: 419.90492
• Product Categories: 1,3,5-triazine
• Mol File: 182918-13-4.mol
• Article Data: 18

Chemical Properties

• Melting Point: 215.0 to 219.0 °C
• Boiling Point: 649.6±58.0 °C(Predicted)
• Appearance: /
• Density: 1.227±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 0.28±0.10(Predicted)
• CAS DataBase Reference: 2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine(182918-13-4)
• EPA Substance Registry System: 2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine(182918-13-4)

Safety Data

• Hazardous Substances Data: 182918-13-4(Hazardous Substances Data)

Usage

Description

2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine is an organic compound characterized by its unique molecular structure, which features two biphenyl groups attached to a triazine core with a chlorine atom at the 6th position. This structure endows the compound with specific properties that make it suitable for various applications in different industries.

Uses

Used in Photoelectric Materials:
2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine is used as a key component in the development of photoelectric materials due to its ability to absorb and emit light efficiently. Its molecular structure allows for the manipulation of light at the molecular level, making it a valuable asset in the creation of advanced optoelectronic devices.
Used in Semiconductor Building Blocks:
In the semiconductor industry, 2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine serves as a crucial building block for the fabrication of semiconductor devices. Its electronic properties and stability contribute to the performance and reliability of these devices, enabling the development of more efficient and advanced semiconductor technologies.
Used in Synthetic Material Intermediates:
2,4-Bis([1,1'-biphenyl]-4-yl)-6-chloro-1,3,5-triazine also plays a significant role as an intermediate in the synthesis of various synthetic materials. Its versatile chemical structure allows for further functionalization and modification, leading to the creation of a wide range of materials with tailored properties for specific applications across different industries.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 92-66-0 4-bromo-1,1'-biphenyl 
• 3315-91-1 4-biphenylylmagnesium bromide 
• 92-52-4 biphenyl 
• 1201-71-4 4-biphenyllithium 
• 10202-45-6 2‐{[1,1'‐biphenyl]‐4‐yl}‐4,6‐dichloro‐1,3,5‐triazine 
• 5122-94-1 4-biphenylboronic acid 
• 2920-38-9 4-cyano-1,1'-biphenyl 

Downstream Products

• 1073062-67-5 2,4-bis(biphenyl-4-yl)-6-(3,5-dibromophenyl)-1,3,5-triazine 

Relevant articles and documents

A simple synthetic method of a 1,3,5-triazine UV absorbent CGL-479 and its characterization

As a novel ultraviolet (UV) absorbent with excellent performance in UVA section (320 ～ 400 nm), 2-{2-hydroxy-4-[(octyloxycarbonyl)ethylideneoxy]phenyl}-4,6-Bis(4-biphenylyl)-1,3,5-triazine (CGL-479) was synthesized in a simple method with a total yield of 45.3% in four steps. Its outstanding UV absorption capability (λmax = 326 nm, ε max = 4.15×104 L·mol-1 ·cm-1), high thermostability [T5 (the temperature of losing 5% in weight) = 385 °C], and compatibility with polymer materials make it a potential substitute of the traditional UV absorbents.

Preparation method of diaryl-substituted chlorotriazine OLED intermediate

The invention provides a preparation method of a diaryl-substituted chlorotriazine OLED intermediate, and the method comprises the following steps: S1, carrying out heating reaction on an aryl nitrile compound and urea in an organic solvent under the action of strong alkali, and carrying out intermolecular ring closing to form a diaryl hydroxyl triazine compound; S2, enabling the diaryl hydroxyl triazine compound obtained in the step S1 to be subjected to a reaction under the action of phosphorus oxychloride, and obtaining the diaryl chlorinated triazine compound. According to the method, the final product can be obtained only through two-step reaction, raw materials are cheap, and expensive catalysts are not needed. The method has the characteristics of low cost, few steps, high yield, few three wastes, easiness in operation, environment friendliness, suitability for industrialization and the like.

ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

The invention provides an organic photoelectric device and a display device. An organic optoelectronic device and a display device including the same are disclosed. The organic photoelectric device includes an anode and a cathode opposite to each other, a light emitting layer between the anode and the cathode, a hole transport layer between the anode and the light emitting layer, and a hole transport auxiliary layer between the light emitting layer and the hole transport layer, wherein the light emitting layer includes a composition including a first compound represented by Chemical Formula 1and a second compound represented by Chemical Formula 2, and the hole transport auxiliary layer includes a third compound represented by Chemical Formula 3. Detailed description of Chemical Formulae 1to 3 is the same as described in the specification.