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2,3-Naphthalenediamine, N,N'-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69905-74-4

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69905-74-4 Usage

General Description

2,3-Naphthalenediamine, N,N'-diphenyl- is a chemical compound that is used in the production of dyes and pigments, as well as in the formulation of adhesives and sealants. It is a solid, crystalline substance that is insoluble in water and is typically used in its powdered form. 2,3-Naphthalenediamine, N,N'-diphenyl- is known to be toxic if ingested or inhaled, and can cause skin and eye irritation upon contact. It is important to handle this chemical with caution and to ensure proper protective equipment and ventilation when working with it. Additionally, proper disposal and handling procedures should be followed to minimize environmental impact and health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 69905-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,0 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69905-74:
(7*6)+(6*9)+(5*9)+(4*0)+(3*5)+(2*7)+(1*4)=174
174 % 10 = 4
So 69905-74-4 is a valid CAS Registry Number.

69905-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,3-N-diphenylnaphthalene-2,3-diamine

1.2 Other means of identification

Product number -
Other names N.N'-Diphenyl-naphthylendiamin-(2.3)

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:69905-74-4 SDS

69905-74-4Downstream Products

69905-74-4Relevant academic research and scientific papers

Transition metal complexes comprising carbene ligands serving as emitters for organic light-emitting diodes (OLED's)

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Page/Page column 34; 35; 36, (2020/03/14)

Use of transition metal complexes of the formula (I) in organic light-emitting diodes where: M1 is a metal atom; carbene is a carbene ligand; L is a monoanionic or dianionic ligand; K is an uncharged monodentate or bidentate ligand selected from the group consisting of phosphines; CO; pyridines; nitriles and conjugated dienes which form a π complex with M1; n is the number of carbene ligands and is at least 1; m is the number of ligands L, where m can be 0 or ≥1; o is the number of ligands K, where o can be 0 or ≥1; where the sum n+m+o is dependent on the oxidation state and coordination number of the metal atom and on the denticity of the ligands carbene, L and K and also on the charge on the ligands carbene and L, with the proviso that n is at least 1, and also an OLED comprising these transition metal complexes, a light-emitting layer comprising these transition metal complexes, OLEDs comprising this light-emitting layer, devices comprising an OLED according to the present invention, and specific transition metal complexes comprising at least two carbene ligands.

Diversity of the quaternary ammonium salt of the imidazole aryl and and its preparation method and application

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Paragraph 0136; 0137; 0138; 0139; 0140, (2016/11/24)

The present invention discloses a diverse arylimidazole quaternary ammonium salt, a preparation method and an application thereof. The diverse arylimidazole quaternary ammonium salt is a compound represented by a formula (L-n'). The diverse arylimidazole quaternary ammonium salt has the following beneficial effects that: the diverse arylimidazole quaternary ammonium salt can be prepared through the one-pot method and is not prepared in a glove box, the raw material (aliphatic or aromatic imine) is subjected to the reaction, the yield is 78-94%, and the target product with high optical purity dr of more than 98:2 is obtained. According to the present invention, operations can be simplified, the yield can be increased, importantly an application range of the compound is expanded, and wide versatility is provided.

ELECTROLUMINESCENT IMIDAZO-QUINOXALINE CARBENE METAL COMPLEXES

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Page/Page column 211; 212, (2016/04/04)

Metal carbene complexes comprising at least one imidazo-quinoxaline ligand, organic electronic devices, especially OLEDs (Organic Light- Emitting Diodes) which comprise such complexes, a light-emitting layer comprising at least one inventive metal carbene complex, an apparatus selected from the group consisting of illuminating elements, stationary visual display units and mobile visual display units comprising such an OLED, the use of such a metal carbene complex for electrophotographic photoreceptors, photoelectric converters, organic solar cells (organic photovoltaics), switching elements, organic light emitting field effect transistors (OLEFETs), image sensors, dye lasers and electroluminescent devices and a process for preparing such metal carbene complexes.

Enlarging the π system of phosphorescent (C^C*) cyclometalated platinum(II) NHC complexes

Tronnier, Alexander,Poethig, Alexander,Metz, Stefan,Wagenblast, Gerhard,Muenster, Ingo,Strassner, Thomas

, p. 6346 - 6356 (2014/07/07)

Cyclometalated (C^C*) platinum(II) N-heterocyclic carbene (NHC) complexes are emerging as a new class of phosphorescent emitters for the application in organic light-emitting devices (OLEDs). We present the synthesis of six new complexes of this class to

Facial and practical synthesis of benzimidazole-based N-heterocyclic carbenes

Wang, Han,Xia, Yuyu,Lv, Shang,Xu, Jingli,Sun, Zhihua

supporting information, p. 2124 - 2127 (2013/05/08)

An efficient synthesis of benzimidazole-based N-heterocyclic carbenes has been developed. The key step in this synthetic methodology was a one-pot protocol for the synthesis of N,N′-diarylaryldiamines starting from aryldiamine and aryl halides.

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