1700-02-3

Product Name2,4-Dichloro-6-phenyl-1,3,5-triazine
Molecular FormulaC₉H₅C_l2N₃
Molecular Weight226.06
Purity99%

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CasNo： 1700-02-3
Molecular Formula： C₉H₅C_l2N₃
Purity： 99%

Industrial Grade,High Purity 2,4-Dichloro-6-phenyl-1,3,5-triazine 1700-02-3 Good Price

1700-02-3 Name
Name	2,4-Dichloro-6-phenyl-1,3,5-triazine
Synonym	2,4-Dichloro-6-phenyl-1,3,5-triazine 98%;4,6-DICHLORO-2-PHENYL TRIAZINE;1,3,5-TRIAZINE-2,4-DICHLORO, 6-PHENYL-;2,4-DICHLORO-6-PHENYL-1,3,5-TRIAZINE;2-[(4-AMINO-3-CHLORO)BENZOYL]BENZOIC ACID;2,4-Dichloro-Phenyl-1,3,5-Triazine;2-Phenyl-4,6-dichlorotriazine;4,6-Dichloro-2-phenyl-1,3,5-triazine

1700-02-3 Chemical & Physical Properties
Melting point	121 °C
Boiling point	427.5±28.0 °C at 760 mmHg
Density	1.4±0.1 g/cm3
Molecular Formula	C9H5Cl2N3
Molecular Weight	226.062
Flash Point	244.9±9.6 °C
PSA	38.67000
LogP	3.18
Exact Mass	224.986053
Vapour Pressure	0.0±1.0 mmHg at 25°C
Index of Refraction	1.610

1700-02-3 Usage

2,4-Dichloro-6-phenyl-1,3,5-triazine,White to Orange to Green powder to crystal, is a heterocyclic derivative and can be used as intermediate of synthetic materials.

InChI:InChI=1/C9H5Cl2N3/c10-8-12-7(13-9(11)14-8)6-4-2-1-3-5-6/h1-5H

1700-02-3 Relevant articles

Synthesis, photophysical and electrochemical properties of novel carbazole-triazine based high triplet energy, solution-processable materials

Oner, Saliha,Aydemir, Murat,Yesil, Fatih,Sahin, Cigdem,Varlikli, Canan

, p. 92 - 99 (2018)

A series of molecules; tBuCz1SiTrz, tBuCz2SiTrz and tBuCz3SiTrz, which contain carbazole unit as hole-transporting group (donor-D) and triazine unit as electron transporting group (acceptor-A) were synthesized and characterized as high-triplet energy (>2.9 eV), solution-processable bipolar emitting materials. Photophysical, electrochemical and computational characterizations addressed that tBuCz2SiTrz has the weakest ICT character, highest photoluminescence quantum yield (PLQY) and charge balance.

Synthesis, Structure, Photoluminescence, and Electroluminescence of Four Europium Complexes: Fabrication of Pure Red Organic Light-Emitting Diodes from Europium Complexes

Karimi Behzad, Sara,Amini, Mostafa M.,Ghanbari, Mohammad,Janghouri, Mohammad,Anzenbacher, Pavel,Ng, Seik Weng

, p. 3644 - 3654 (2017)

Four new europium complexes were prepared by treating europium(III) trifluoro(thenoyl)acetonate trihydrate with new tridentate ligands, based on dipyrazolyltriazine and utilized as emitting materials in electroluminescent devices.

Preparation and application of novel electron acceptor material

-

Paragraph 0016; 0017, (2021/07/31)

The invention belongs to the technical field of organic electroluminescent devices, and discloses a novel electron-deficient acceptor material and an application thereof in organic electroluminescent devices.

Polymerizable UV absorbers for the UV stabilization of polyesters. I. Design, synthesis and polymerization of a library of UV absorbing monomers

Cormack, Peter A.G.,Erdemli, Omer C.,Sankey, Stephen W.

, (2021/10/14)

UV stabilizers, such as Tinuvin 1577, are organic additives that are used in the polymer industry to suppress polymer photodegradation, however leaching of the stabilizers from polymers is a significant practical issue which limits the effectiveness of the stabilizers and restricts polymer lifetimes.

Crystal Structure and Subsequent Ligand Design of a Nonriboside Partial Agonist Bound to the Adenosine A2AReceptor

Amelia, Tasia,Van Veldhoven, Jacobus P. D.,Falsini, Matteo,Liu, Rongfang,Heitman, Laura H.,Van Westen, Gerard J. P.,Segala, Elena,Verdon, Grégory,Cheng, Robert K. Y.,Cooke, Robert M.,Van Der Es, Daan,Ijzerman, Adriaan P.

, p. 3827 - 3842 (2021/05/04)

In this study, we determined the crystal structure of an engineered human adenosine A2A receptor bound to a partial agonist and compared it to structures cocrystallized with either a full agonist or an antagonist/inverse agonist.

Organic compound, and organic electroluminescent device and electronic device using same

-

Paragraph 0164-0169, (2021/02/20)

The invention relates to an organic compound. The structure of the organic compound comprises a formula I. When the organic compound provided by the invention is used for a light-emitting layer of anorganic electroluminescent device, the device efficiency of the device can be effectively improved, and the service life of the organic electroluminescent device is prolonged.

1700-02-3 Process route

: 108-77-0
1,3,5-trichloro-2,4,6-triazine

: phenylmagnesium bromide

: 1700-02-3
2,4-dichloro-6-phenyl-1,3,5-triazine

: 3842-55-5
2-chloro-4,6-diphenyl-1,3,5-triazine

Conditions

Conditions	Yield
With diethyl ether;

: 108-77-0
1,3,5-trichloro-2,4,6-triazine

: 98-80-6
phenylboronic acid

: 1700-02-3
2,4-dichloro-6-phenyl-1,3,5-triazine

Conditions

Conditions	Yield
With potassium carbonate; In ethanol; water; at 27 - 30 ℃; for 1h; Irradiation;	92%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 24h;	85%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In tetrahydrofuran; water; toluene; for 9h; Reflux;	84%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In 1,4-dioxane; water; toluene; for 9h; Reflux;	84%
With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; In toluene; at 60 ℃; for 12h; Inert atmosphere; Schlenk technique;	82%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 10h; Inert atmosphere;	80.4%
With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; In toluene; for 10h; Inert atmosphere; Reflux;	80%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 10h;	75.4%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 10h; Inert atmosphere;	75.4%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In tetrahydrofuran; water; at 80 ℃; for 10h; Inert atmosphere;	75.4%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; water; at 90 ℃;	60%
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydroxide; In tetrahydrofuran; water;