2028-76-4

Basic information

• Product Name: 3-Nitrobenzenediazonium·chloride
• Synonyms: 3-Nitrobenzenediazonium·chloride
• CAS NO: 2028-76-4
• Molecular Formula: C₆H₄N₃O₂*Cl
• Molecular Weight: 185.57
• Mol File: 2028-76-4.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• Density: 1.8436 (rough estimate)
• Refractive Index: 1.5870 (estimate)
• CAS DataBase Reference: 3-Nitrobenzenediazonium·chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Nitrobenzenediazonium·chloride(2028-76-4)
• EPA Substance Registry System: 3-Nitrobenzenediazonium·chloride(2028-76-4)

Safety Data

• Hazardous Substances Data: 2028-76-4(Hazardous Substances Data)

Upstream product

• 99-09-2 3-nitro-aniline 
• 58364-71-9 3-methyl-2-[(1Ξ,2E)-(3-nitro-phenyl)-triazenylidene]-2,3-dihydro-benzothiazole 
• 58364-65-1 3-methyl-2-[(1Ξ,2Z)-(3-nitro-phenyl)-triazenylidene]-2,3-dihydro-benzothiazole 
• 110-46-3 isopentyl nitrite 

Downstream Products

• 70600-02-1 1-nitro-3-(2,2-diphenylethenyl)benzene 
• 124525-54-8 2-methyl-3-(3-nitrophenyl)propenoic acid 
• 3662-36-0 5-methyl-3-[3-(3-nitro-phenyl)-triazenyl]-isoxazole 
• 94783-65-0 3,4-dimethyl-4-(3-nitro-phenylazo)-4H-isoxazol-5-one 
• 84705-50-0 5-Hydroxy-4,9-dimethoxy-6-(3-nitro-phenylazo)-furo[3,2-g]chromen-7-one 
• 76383-48-7 4-Butyl-4-(3-nitro-phenylazo)-1,2-diphenyl-pyrazolidine-3,5-dione 
• 78818-67-4 1-(m-nitrophenyl)-3,5-diphenylformazan 
• 148839-72-9 α-thiocarboxamido-α-(3-nitrophenyl)hydrazonoacetonitrile 
• 28359-26-4 2-(3-Nitro-phenyl)-1-phenyl-isothiourea 
• 18794-99-5 2-[(3-Nitro-phenyl)-hydrazono]-3-oxo-butyric acid ethyl ester 
• 98-95-3 nitrobenzene 

Relevant articles and documents

Experimental and theoretical studies of azo derivatives in terms of different donors, acceptors and position isomerism: Synthesis, characterization and a combined electronic absorption, electrochemical and DFT study

Eight azo derivatives with two donor groups- diphenylamine and N,N-dimethylphenyl, and four acceptor groups - 3-nitrophenyl, 4-nitrophenyl, 4-phenylcarboxylic acid, and 3-phenylcarboxylic acid, were synthesized and characterized using 1H-NMR an

3-Aminopyrazolo[4,3-c]pyridine-4,6-dione as a precursor for novel pyrazolo[4,5,1-ij][1,6]naphthyridines and pyrido[4’,3’:3,4]pyrazolo[1,5-a]pyrimidines

The versatile, 3-aminopyrazolo[4,3-c]pyridine-4,6-dione (2) was synthesized and allowed to react with aldehydes, aryldiazonium chlorides, chalcones and enaminones to afford regioselectively the novel pyrazolo[4,3-c]pyridine derivatives 4a-c, pyrazolo[4,5,

Synthesis and properties of new N, N′ - phenyltetrazole podand

The synthesis of a new chromogenic N,N′-phenyltetrazole receptor is reported here. The cationbinding properties of this receptor in solution were investigated by naked-eye colour change, electrochemical methods and UV-Vis spectroscopy in various solvents