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10311-62-3

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10311-62-3 Usage

General Description

N4,N4'-di-naphthalen-2-yl-biphenyl-4,4'-diamine is a chemical compound used in the production of polymers, particularly in the manufacturing of polyurethane and epoxy resins. It is commonly used as an antioxidant and stabilizer in various industrial applications, including the production of rubber, plastics, and adhesives. N4,N4'-DI-NAPHTHALEN-2-YL-BIPHENYL-4,4'-DIAMINE is known for its ability to protect materials from degradation caused by heat, light, and oxygen exposure, making it an important additive in the production of long-lasting and durable synthetic materials. Additionally, it has been studied for its potential use in medical applications, including as a component in drug delivery systems and in the development of new medical devices.

Check Digit Verification of cas no

The CAS Registry Mumber 10311-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10311-62:
(7*1)+(6*0)+(5*3)+(4*1)+(3*1)+(2*6)+(1*2)=43
43 % 10 = 3
So 10311-62-3 is a valid CAS Registry Number.

10311-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-[4-(naphthalen-2-ylamino)phenyl]phenyl]naphthalen-2-amine

1.2 Other means of identification

Product number -
Other names N4,N4'-Di-naphthalen-2-yl-biphenyl-4,4'-diamine

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:10311-62-3 SDS

10311-62-3Downstream Products

10311-62-3Relevant articles and documents

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT HAVING BENZOCYCLOBUTENE FUNCTIONAL GROUP FOR CROSS-LINKED BOND, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

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Paragraph 0267; 0273-0277, (2021/09/14)

[1] An organic compound for forming 2 an organic thin film is disposed between the first electrode and the second electrode of the organic electronic element. It is characterized in that it comprises at least one benzocyclobutene group (benzocyclobutene) at its terminal.

Metal-Free Oxidative C-C Coupling of Arylamines Using a Quinone-Based Organic Oxidant

Maddala, Sudhakar,Mallick, Sudesh,Venkatakrishnan, Parthasarathy

, p. 8958 - 8972 (2017/09/11)

A variety of arylamines are shown to undergo oxidative C-C bond formation using quinone-based chloranil/H+ reagent as the recyclable organic (metal-free) oxidant system to afford benzidines/naphthidines. Arylamines (3°/2°) designed with various substituents were employed to understand the steric as well as electronic preferences of oxidative dimerization, and a mechanism involving amine radical cation has been proposed. The tetraphenylbenzidine derivative obtained via oxidative C-C coupling has been further converted to blue-emissive hole-transporting material via a simple chemical transformation. This study highlights the preparation of novel HTMs in a simple, economic, and efficient manner.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT EMPLOYING THE SAME

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Page/Page column 37, (2010/02/13)

Provided are an aromatic amine compound represented by the following Formula (1) and an organic electroluminescent element which has at least one organic thin film layer containing the above aromatic amine derivative in the form of a single component. The organic electroluminescent element described above has a high luminescent efficiency even at a low voltage and a long life. It can emit blue light even at high temperatures. In Formula (1), Ar1 and Ar2 each represent naphthyl and the like; Ar3 to Ar6 each represent phenyl, naphthyl, phenanthryl and the like; Ar7 to Ar10 each represent 1,4-phenylene and the like; L represents a single bond and the like; provided that the conditions of (1) and/or (2) are satisfied:(1) at least one of Ar3 to Ar6 is a condensed aryl group having 10 to 50 nuclear carbon atoms and(2) at least one of Ar1 and Ar2 is a condensed aryl group having 12 to 50 nuclear carbon atoms.

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