4572-48-9

Basic information

• Product Name: 1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]-
• CAS NO: 4572-48-9
• Molecular Formula: C20H21N
• Molecular Weight: 275.393
• Mol File: 4572-48-9.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]-(4572-48-9)
• EPA Substance Registry System: 1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]-(4572-48-9)

Safety Data

• Hazardous Substances Data: 4572-48-9(Hazardous Substances Data)

Usage

General Description

1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]- is a chemical compound with the molecular formula C22H21N. It is a derivative of naphthalene and belongs to the class of organic compounds known as anilines. This chemical is often used in the manufacturing of dyes, pharmaceuticals, and other organic substances. It is a colorless to pale yellow solid with a faint odor, and it is considered to be slightly soluble in water. 1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]- is also known by its trade name 4-tert-Butylaniline, and it is important to handle this chemical with caution due to its potential health hazards.

Upstream product

• 769-92-6 4-tert-Butylaniline 
• 134-32-7 1-amino-naphthalene 
• 87797-38-4 p-t-butylphenyl 1-naphthyl nitroxide 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 86-53-3 1-Cyanonaphthalene 
• 344871-83-6 N-(4-tert-Butyl-phenyl)-N-naphthalen-1-yl-hydroxylamine 
• 6637-03-2 1-(tert-butyl)-4-nitrosobenzene 
• 90-11-9 1-Bromonaphthalene 

Downstream Products

• 1119083-63-4 N₁,N₃-bis(4-tert-butylphenyl)-N₁,N₃-bis(naphthalen-1-yl)-5-(thiophen-2-yl)benzene-1,3-diamine 
• 1262436-23-6 N-(4-tert-butylphenyl)-N-(naphthalen-1-yl)-7,8,9,10-tetraphenylfluoranthen-3-amine 
• 89444-26-8 4,4'-bis(N-t-butylphenyl-N-acetyl)amino-1,1'-binaphthyl 
• 87797-56-6 N-p-t-butylphenyl-1,4-naphthoquinone imine 
• 89444-27-9 N-p-t-butylphenyl-2-(p-t-butylanilino)-1,4-naphthoquinone imine 

Relevant articles and documents

Nickel-Catalyzed Amination of Aryl Nitriles for Accessing Diarylamines through C?CN Bond Activation

A nickel-catalyzed amination to access diarylamines has been developed through C?CN bond activation of aryl nitriles with anilines. In this developed catalytic protocol, various aromatic and heteroaromatic nitriles could be utilized as the electrophiles to couple with substituted anilines. A diversity of diarylamines were obtained in 15–95% yields. (Figure presented.).

Nitrogen-containing compound, organic electroluminescent device, and electronic device

The invention provides a nitrogen-containing compound, an organic electroluminescent device and an electronic device, and belongs to the technical field of organic materials. The structure of the nitrogen-containing compound is represented by Chemical Formula 1: wherein X1, X2, Y1, Y2 are the same or different from each other and are each independently a single bond, O, S, N(R3), C(R4R5), Ge(R6R7), Si(R8R9), Se, wherein X1 and Y1 are not single bonds simultaneously and X2 and Y2 are not single bonds simultaneously.

Compound, organic electroluminescent device, and electronic device

The present invention belongs to the technical field of organic materials, and provides a compound having a structure represented by a chemical formula 1, wherein Ar1, Ar2, Ar3, and Ar4 are H or a group represented by a chemical formula 1-1, and at least one of Ar1, Ar2, Ar3, and Ar4 is a group represented by a chemical formula 1. The invention provides a compound taking a phenanthrene fused ringderivative as a parent nucleus, and the compound molecules have very strong planarity. The strong planarity of compound molecules can enhance the rigidity of the material and can prolong the service life of the material. Besides, the molecular parent nucleus and the triarylamine group are easy to form a large conjugated system, the intramolecular electron cloud density is increased, the HOMO energy level can be further adjusted to a proper level, the electron mobility and the transition rate are further improved, and the organic light-emitting device has high device efficiency. The invention also provides an organic electroluminescent device and an electronic device comprising the compound.