2125473-29-0

Basic information

• Product Name: 2-Chloro-4-(3-chloro-phenyl)-6-phenyl-[1,3,5]triazine
• Synonyms: 2-Chloro-4-(3-chloro-phenyl)-6-phenyl-[1,3,5]triazine
• CAS NO: 2125473-29-0
• Molecular Formula: C15H9Cl2N3
• Molecular Weight: 302.15806
• EINECS: -0
• Mol File: 2125473-29-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 517.4±52.0 °C(Predicted)
• Appearance: /
• Density: 1.351±0.06 g/cm3(Predicted)
• PKA: -0.59±0.10(Predicted)
• CAS DataBase Reference: 2-Chloro-4-(3-chloro-phenyl)-6-phenyl-[1,3,5]triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloro-4-(3-chloro-phenyl)-6-phenyl-[1,3,5]triazine(2125473-29-0)
• EPA Substance Registry System: 2-Chloro-4-(3-chloro-phenyl)-6-phenyl-[1,3,5]triazine(2125473-29-0)

Safety Data

• Hazardous Substances Data: 2125473-29-0(Hazardous Substances Data)

Usage

Uses

2-Chloro-4-(3-chloro-phenyl)-6-phenyl-[1,3,5]triazine is a useful research chemical.

Upstream product

• 618-48-4 3-chlorobenzamide 
• 1670-14-0 benzamidine monohydrochloride 
• 74703-17-6 3-chlorobenzoyl isocyanate 
• 1700-02-3 2,4-dichloro-6-phenyl-1,3,5-triazine 
• 63503-60-6 3-chlorophenylboronic acid 
• 618-46-2 m-Chlorobenzoyl chloride 
• 17513-09-6 N′-cyanobenzamidine 
• 24167-52-0 N,N-dimethyl-3-chlorobenzamide 
• 535-80-8 3-chlorobenzoate 

Downstream Products

• 1238752-26-5 ((C₆H₄)((CH₃)4(C₂O₂B)))2(C₃N₃)(C₆H₅) 

Relevant articles and documents

Scalable Synthetic Strategy for Unsymmetrical Trisubstituted s-Triazines

A scalable synthetic strategy to produce a large variety of unsymmetrical trisubstituted 1,3,5-triazines was developed. This protocol applied in situ formed acyl isocyanate from amide to react with amidine, introducing two substituents to the 1,3,5-triazinone ring with a low production cost and a simple workup procedure. The scalability of this method was demonstrated by translating a small-scale procedure to a multi-kilogram-scale synthesis. Chlorination and a further coupling reaction with various nucleophiles could provide unsymmetrical trisubstituted 1,3,5-triazines bearing diverse functional groups.

Organic Electronic Device Comprising an Organic Semiconductor Layer and a Device

The present invention relates to a compound of formula 1 and an organic electronic device comprising an organic semiconductor layer, wherein at least one organic semiconductor layer comprises a compound of formula (1), wherein X is selected from O, S or Se; Ar1 is selected from unsubstituted or substituted C2 to C60 heteroarylene, and wherein the substituted C2 to C60 heteroarylene comprises at least about one to about six substituents, wherein the substituent of the substituted C2 to C60 heteroarylene are independently selected from C1 to C12 alkyl, C1 to C12 alkoxy, CN, OH, halogen, C6 to C36 arylene, or C2 to C25 heteroarylene; n is 1 or 2; L1 is selected from a single bond, C1 to C4 alkyl, substituted or unsubstituted C6 to C36 arylene, wherein the substituent of substituted C6 to C36 arylene is selected from C1 to C12 alkyl, C6 to C18 arylene; L2 is selected from a single bond or C1 to C6 alkyl; R1, R2 are independently selected from substituted or unsubstituted C1 to C16 alkyl, wherein the substituent of substituted C1 to C16 alkyl is selected from C6 to C18 arylene or C2 to C12 heteroarylene; wherein the compound of formula 1 comprises at least about 4 of C6-arylene rings and a molecular mass of at least about 400 g/mol to about 1800 g/mol.

Novel hetero-cyclic compound and organic light emitting device comprising the same

The present invention relates to a novel heterocyclic compound capable of increasing efficiency, low driving voltage and/or lifetime characteristics in an organic light emitting device, and an organic light emitting device using the same. The novel heterocyclic compound is represented by chemical formula 1. In chemical formula 1, L is phenylene, biphenylylene, or naphthylene, and Xs are each independently N or CH, wherein at least one of Xs is N.COPYRIGHT KIPO 2019