19291-76-0

Usage

Uses

Used in Chemical Synthesis Industry:
1,2-Naphthalenedicarbonitrile is used as a precursor for the synthesis of various derivative compounds, such as dyes, pigments, and pharmaceuticals. Its unique chemical structure allows for the creation of a wide range of products with diverse applications.
Used in Research Settings:
In research, 1,2-Naphthalenedicarbonitrile serves as a valuable compound for studying the properties and reactions of naphthalene derivatives. It can be used to explore new synthetic pathways, investigate the effects of structural modifications, and develop novel applications in various fields.

InChI:InChI=1/C12H6N2/c13-7-10-6-5-9-3-1-2-4-11(9)12(10)8-14/h1-6H

Upstream product

• 100-42-5 styrene 
• 1071-98-3 2-butynedinitrile 
• 74-90-8 hydrogen cyanide 
• 42976-05-6 N,N'-bis(phenylsulfonyl)-1,4-naphthoquinone diimine 
• 858499-39-5 4-benzenesulfonylamino-naphthalene-1,2-dicarbonitrile 
• 98-81-7 1-bromovinylbenzene 
• 764-42-1 1,2-Dicyanoethylene 
• 143-33-9 sodium cyanide 
• 4379-50-4 1H-benzo[e]isoindole-1,3(2H)-dione 
• 7664-41-7 ammonia 
• 129278-19-9 1-Bromo-2-naphthylazo phenyl sulfide 
• 10442-39-4 tetra-n-butylammonium cyanide 
• 858463-70-4 4-amino-naphthalene-1,2-dicarbonitrile 

Downstream Products

• 1338975-68-0 B(OC₆H₅)(C₁₀H₆C₂N₂)3 
• 109297-25-8 4-(p-tolylsulphonylmethyl)naphthalene-1,2-dicarbonitrile 
• 2088-87-1 naphthalene-1,2-dicarboxylic acid 

Relevant academic research and scientific papers

Synthesis, spectroscopic, and electrochemical studies of 1,2-naphthalene-ring-fused tetraazachlorins, -bacteriochlorins, and -isobacteriochlorins: The separation and characterization of structural isomers

1,2-Naphthalene-ring-expanded tetraazachlorins (TACs), tetraazabacteriochlorins (TABCs), and tetraazaisobacteriochlorins (TAiBCs) have been synthesized. Procedures for the synthesis of the starting materials, that is, derivatives of 1,2-naphthalene-dicarb

SRN1 SYNTHESES OF BIS(PHENYLTHIO)- AND DICYANO-NAPHTHALENES VIA DIAZOSULFIDES

The reactions of bromonaphthalenediazonium tetrafluoroborates (6a,b and 11a,b) with sodium benzenethiolate in DMSO give, through the preliminary formation of the corresponding diazosulfides (7a,b and 12a,b) bis(phenylthio)naphthalenes (8a,b and 13a,b) deriving from substitution of both the diazo group and the bromine.Isolated diazosulfides (7a,b and 12a,b) likewise furnish satisfactory yields of dinitriles (9a,b and 14a,b) by reaction with excess tetrabutylammonium cyanide in DMSO under photostimulation by a sunlamp.The intervention of an SRN1 process accounting for the formation of the disubstitution products is postulated.