14368-49-1

Basic information

• Product Name: 4-nitrobenzenediazonium
• Synonyms: FastScarletGgSaltC.I.37010;Benzenediazonium, 4-nitro- (9CI);4-nitrophenyldiazonium
• CAS NO: 14368-49-1
• Molecular Formula: C₆H₄N₃O₂
• Molecular Weight: 150.11486
• EINECS: 238-340-9
• Product Categories: NITRO
• Mol File: 14368-49-1.mol
• Article Data: 11

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 4-nitrobenzenediazonium(CAS DataBase Reference)
• NIST Chemistry Reference: 4-nitrobenzenediazonium(14368-49-1)
• EPA Substance Registry System: 4-nitrobenzenediazonium(14368-49-1)

Safety Data

• Hazardous Substances Data: 14368-49-1(Hazardous Substances Data)

Usage

Description

4-nitrobenzenediazonium is an aromatic diazonium ion derived from the diazotization of the amino group in 4-nitroaniline. It is a chemical compound with a specific structure and properties that make it useful in various applications.

Uses

Used in Chemical Synthesis:
4-nitrobenzenediazonium is used as an intermediate in the synthesis of various organic compounds. Its reactivity and stability allow it to be a versatile building block for the creation of a wide range of molecules, including dyes, pharmaceuticals, and other specialty chemicals.
Used in Dye Production:
In the dye industry, 4-nitrobenzenediazonium is used as a precursor for the production of various dyes. Its ability to form colored compounds makes it a valuable component in the development of new dyes with specific color properties and applications.
Used in Analytical Chemistry:
4-nitrobenzenediazonium is employed as a reagent in analytical chemistry for the detection and identification of certain functional groups. Its unique chemical properties enable it to react selectively with specific compounds, providing a means to analyze and characterize various substances.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-nitrobenzenediazonium is used as a starting material for the development of new drugs. Its structural features and reactivity make it a promising candidate for the synthesis of novel therapeutic agents with potential applications in the treatment of various diseases and conditions.
Used in Material Science:
4-nitrobenzenediazonium is utilized in the field of material science for the development of new materials with specific properties. Its ability to form stable complexes and its reactivity make it a valuable component in the creation of advanced materials with applications in electronics, optics, and other high-tech industries.

InChI:InChI=1/C6H4N3O2.BF4/c7-8-5-1-3-6(4-2-5)9(10)11;2-1(3,4)5/h1-4H;/q+1;-1

Upstream product

• 16020-14-7 (E)-1-methoxy-2-(4-nitrophenyl)diazene 
• 7227-92-1 3,3-dimethyl-1-(4-nitrophenyl)triazene 
• 58142-01-1 E 4-nitrobenzenediazotate anion 
• 58692-49-2 isopropyl (E)-p-nitrophenylazo ether 
• 82944-47-6 C₉H₇N₃O₃ 
• 82952-88-3 t-butyl 4-nitrophenylazo ether 
• 82944-48-7 benzyl (E)-p-nitrophenylazo ether 
• 100-01-6 4-nitro-aniline 
• 40078-29-3 4-nitro-benzene-standard diazotate 
• 40078-29-3 4-nitro-benzenediazo hydroxide 
• 17032-11-0 anilinium 
• 62-53-3 aniline 

Downstream Products

• 93937-78-1 (E)-2-(p-nitrophenylazo)imidazole 
• 92166-66-0 3,4-Dimethyl-2-(4-nitro-phenylazo)-phenol 
• 106167-09-3 benzothiazole-2-carbaldehyde (4-nitro-phenyl)-hydrazone 
• 41554-75-0 2-(4-nitro-phenyl)-2H-[1,2,3]triazolo[4,5-f]quinoline 
• 61800-67-7 furan-2,3,4-trione-3-(4-nitro-phenylhydrazone) 
• 19412-20-5 N-benzothiazol-2-yl-N'-(4-nitro-phenyl)-triazene 
• 873969-44-9 3-hydroxy-6-hydroxymethyl-2-(4-nitro-phenyl)-pyran-4-one 
• 120743-34-2 3-Methoxy-4-(4-nitro-phenylazo)-phenol 
• 100379-31-5 6-(4-nitro-phenylhydrazono)-5-oxo-heptanoic acid 
• 109997-29-7 4-nitro-2-(4-nitrophenylazo)-phenol 
• 84719-24-4 2-phenyl-oxazole-4,5-dione-4-(4-nitro-phenylhydrazone) 

Relevant articles and documents

-

-

Star-shaped molecules containing both azo chromophores and carbazole units as a new type of photoresponsive amorphous material

We synthesized a series of star-shaped molecules containing both azo chromophores and carbazole units (nCz-AZ-X), where n is the number of carbazole units (n = 3 and 6) and X represents cyano (CN) and nitro (NT) as the electron-withdrawing groups on the azobenzenes. The azo compounds existed as amorphous solids at room temperature with glass transition temperatures (T g) of 89, 86, 74 and 73 °C for 3Cz-AZ-CN, 3CZ-AZ-NT, 6Cz-AZ-CN and 6Cz-AZ-NT, respectively. Thin solid films of the azo molecular glasses were obtained by spin-coating. The formation of the photoinduced self-structured surface patterns was investigated by irradiating the solid thin films of the azo molecular glasses with a uniform laser beam (532 nm, 200 mW cm-2) at normal incidence. The formation of surface-relief-gratings (SRGs) was studied by exposing the thin films to an interference pattern of the laser beams (532 nm, 80 mW cm-2). The formation of both the self-structured surface patterns and SRGs showed a close correlation with the electron-withdrawing groups of the azo chromophores and the content of the carbazole units in the molecules. The development of these new star-shaped molecules can add a new member to the category of azo molecular glasses and lead to a deeper understanding of the photoinduced effects and their correlation with molecular structures. The Royal Society of Chemistry 2013.

Micellar catalysis in the systems arylamine-diphenylamine-NO 2-

By methods of UV and IR spectroscopy and thermogravimetry reactions of diazotizaion and azo coupling were studied in the systems of primary arylamine (p-nitro-, p-carboxy- and p-sulfoaniline)- diphenylamine -nitrite ion in water and micellar media on the basis of surfactants. The micellar catalysis effect of sodium dodecylsulfate in the micellar media was revealed. Rate of diazotization was shown to be independent of the surfactants of various types. Formation of ionic associates of azo dyes with dodecylsulfate anions in premicellar region was established and physicochemical characteristics of the associates were estimated.