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

Description

1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]-, also known as 4-tert-Butylaniline, 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 colorless to pale yellow solid with a faint odor is slightly soluble in water and is often used in the manufacturing of dyes, pharmaceuticals, and other organic substances.

Uses

Used in Dye Industry:
1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]is used as an intermediate in the synthesis of dyes for its ability to contribute to the color and stability of the final product.
Used in Pharmaceutical Industry:
1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]is used as a building block in the development of pharmaceuticals, playing a crucial role in the synthesis of various medicinal compounds.
Used in Organic Synthesis:
1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, aiding in the creation of a wide range of organic substances.
It is important to handle 1-Naphthalenamine, N-[4-(1,1-dimethylethyl)phenyl]with caution due to its potential health hazards.

Upstream product

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

Downstream Products

• 89444-27-9 N-p-t-butylphenyl-2-(p-t-butylanilino)-1,4-naphthoquinone imine 
• 87797-56-6 N-p-t-butylphenyl-1,4-naphthoquinone imine 
• 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 

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.

PYRENE DERIVATIVES AND ORGANIC ELECTRO LUMINESCENT DEVICE COMPRISING SAME

The present invention relates to a pyrene based derivative compound of an asymmetric structure and an organic electroluminescent device comprising the same. The pyrene derivative according to the present invention is characterized by being represented by chemical formula A through chemical formula B. The pyrene derivative compound according to the present invention exhibits remarkably improved blue color purity as compared to an organic electroluminescent device using an existing pyrene based aryl amine derivative compound while being able to realize full color since life characteristic and luminance characteristic are excellent, thereby being able to be used in various display devices.