4684-12-2

Usage

Uses

Used in Chemical Synthesis Industry:
1-Amino-4-chloronaphthalene is used as a key intermediate in the synthesis of various organic compounds for its ability to be a building block in the creation of dyes and pharmaceuticals. Its unique structure allows for the development of a range of products with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-amino-4-chloronaphthalene is used as a precursor in the development of new drugs, leveraging its chemical properties to form the basis of potential therapeutic agents.
Used in Dye Industry:
1-Amino-4-chloronaphthalene is used as a starting material for the production of dyes, where its chemical structure contributes to the color and properties of the final dye products.

InChI:InChI=1/C11H8N2S/c1-2-6-13-8-9(12-11(13)5-1)10-4-3-7-14-10/h1-8H

Upstream product

• 24251-12-5 tertiary amyl hypochlorite 
• 890-51-7 N-benzylidenenaphthalen-1-amine 
• 86-57-7 1-Nitronaphthalene 
• 605-61-8 1-chloro-4-nitronaphthalene 
• 1825-31-6 1,4-dichloronaphthalene 
• 84-86-6 4-amino-1-naphthalenesufonic acid 
• 575-36-0 1-acetamidonaphthalene 
• 607-30-7 hydroxynaphthylamine 
• 134-32-7 1-amino-naphthalene 
• 7732-18-5 water 
• 7647-01-0 hydrogenchloride 
• 858005-86-4 2-methyl-5-nitro-benzenesulfonic acid-(4-chloro-[1]naphthylamide) 
• 776-34-1 1-amino-4-nitronaphthalene 
• 108981-71-1 2-methyl-5-nitro-benzenesulfonic acid-[1]naphthylamide 

Downstream Products

• 97027-10-6 N-(2-chloro-ethyl)-N'-(4-chloro-[1]naphthyl)-urea 
• 858005-76-2 N-(4-chloro-[1]naphthyl)-toluene-4-sulfonamide 
• 80961-82-6 C₂₃H₁₇ClN₄O 
• 137840-31-4 2-[(4-Chloro-naphthalen-1-ylcarbamoyl)-methyl]-benzoic acid 
• 134-32-7 1-amino-naphthalene 
• 737-89-3 N,N-di(naphth-1-yl)amine 
• 101670-65-9 4-chloro-1-naphthyl isothiocyanate 
• 1169867-51-9 (Z)-1-(2-bromophenyl)-3-[(4-chloro-1-naphthyl)amino]-3-phenylprop-2-en-1-one 
• 90-13-1 1-Chloronaphthalene 
• 139574-57-5 2-(2-(4-chloronaphthalen-1-yl)hydrazono)-5,5-dimethylcyclohexane-1,3-dione 
• 28785-64-0 4-Chloro-N-(p-<2-(diethylamino)ethoxy>-benzylidene)-1-naphthylamine 

Relevant academic research and scientific papers

SILICON CONTAINING ORGANIC FLUORESCENT MATERIALS

Novel silicon containing compounds for organic electroluminescent devices is disclosed. The compounds can be used as emitters in the emissive layer of the organic electroluminescent device. More specifically, these compounds can emit blue light. The devices incorporating these compounds as emitters show unexpecting higher efficiency and longer lifetime than prior art compounds. Also disclosed is an organic electroluminescent device and a formulation.

Direct cyanation of picolinamides using K4[Fe(CN)6] as the cyanide source

The efficient, simple, and environment-friendly route of direct cyanation of picolinamides has been developed with nontoxic K4[Fe(CN)6] as the cyanide source through Pdcatalyzed C-H bond activation. A series of N-(naphthalene-1- yl)picolinamide derivatives were successfully transformed to the corresponding cyanation products. The cyanation mechanism has also been speculated.