28988-02-5

Basic information

• Product Name: Furan, 2-(2-nitrophenyl)-
• CAS NO: 28988-02-5
• Molecular Formula: C10H7NO3
• Molecular Weight: 189.17
• Mol File: 28988-02-5.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Furan, 2-(2-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Furan, 2-(2-nitrophenyl)-(28988-02-5)
• EPA Substance Registry System: Furan, 2-(2-nitrophenyl)-(28988-02-5)

Safety Data

• Hazardous Substances Data: 28988-02-5(Hazardous Substances Data)

Upstream product

• 110-00-9 furan 
• 577-19-5 2-nitrophenyl bromide 
• 215256-91-0 1-(2-nitrophenyl)buta-2,3-dien-1-one 
• 365-33-3 2-nitrobenzenediazonium tetrafluoroborate 
• 13331-23-2 fur-2-ylboronic acid 
• 88-74-4 2-nitro-aniline 
• 29048-34-8 5-(2-nitrophenyl)-2-furoic acid 
• 609-73-4 o-nitroiodobenzene 
• 118486-94-5 2-(tributylstannyl)furan 

Downstream Products

• 855948-13-9 2-(2-furyl)aniline hydrochloride 
• 1352548-18-5 N-[2-(2-furyl)phenyl]-4-methylbenzenesulfonamide 
• 102269-45-4 2-[(2-Furan-2-yl-phenylamino)-methylene]-malonic acid diethyl ester 
• 55578-79-5 2-(2-aminophenyl)furan 

Relevant articles and documents

LIGHT-EMITTING MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE, ORGANIC ELECTROLUMINESCENT DEVICE USING SAME, AND MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE

Disclosed are a fused compound having excellent emission wavelength control and luminous efficiency, a method for manufacturing the same, and an organic electronic device including the fused compound. Symmetric, asymmetric, and planar structures of the pr

UiO-66 microcrystals catalyzed direct arylation of enol acetates and heteroarenes with aryl diazonium salts in water

UiO-66 is a classic Metal–organic framework (MOF) that constructed by zirconium cations and terephthalate with high chemical and thermal stability. Using pristine UiO-66 nanocrystals as the catalysts, the carbon–carbon bond formation based on denitrogenat

Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl-heteroaryl compounds

A highly regioselective, carbazole based Electron Donor Acceptor (EDA) catalyzed synthesis of biaryl and aryl-heteroaryl compounds is described. Various indole and carbazole derivatives were screened for the Homolytic Aromatic Substitution (HAS) reaction. Tetrahydrocarbazole (THC) was very efficient for the HAS transformation and proceeded via a complex formation between diazonium salt and electron rich tetrahydrocarbazole. The UV-Vis spectroscopy technique has been used to confirm the complex formation. The in situ generated EDA complex even in a catalytic amount is found to be efficient for the Single Electron Transfer (SET) process without any photoactivation. Biaryl compounds, 2-phenylfuran, 2-phenylthiophene, and 2-phenylpyrrole and bioactive compounds such as dantrolene and canagliflozin have been synthesized in moderate to excellent yields.