28289-83-0

Basic information

• Product Name: Benzene, 1-nitro-4-(1-propynyl)- (8CI,9CI)
• Synonyms: Benzene, 1-nitro-4-(1-propynyl)- (8CI,9CI);1-(4-Nitrophenyl)-1-propyne;1-Nitro-4-(1-propynyl)benzene
• CAS NO: 28289-83-0
• Molecular Formula: C₉H₇NO₂
• Molecular Weight: 161.16
• Mol File: 28289-83-0.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzene, 1-nitro-4-(1-propynyl)- (8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-nitro-4-(1-propynyl)- (8CI,9CI)(28289-83-0)
• EPA Substance Registry System: Benzene, 1-nitro-4-(1-propynyl)- (8CI,9CI)(28289-83-0)

Safety Data

• Hazardous Substances Data: 28289-83-0(Hazardous Substances Data)

Upstream product

• 100-19-6 (4-nitrophenyl)ethanone 
• 27491-70-9 dimethyl diazomethylphosphonate 
• 590-93-2 2-Butynoic acid 
• 100-00-5 4-chlorobenzonitrile 
• 636-98-6 p-nitrobenzene iodide 
• 58335-31-2 1,3-dilithiopropyne 
• 1469462-85-8 1-cyano-1-(4-nitrophenyl)ethyl diethyl phosphate 
• 586-78-7 para-nitrophenyl bromide 
• 41412-79-7 1-(3-chloroprop-1-ynyl)-4-nitrobenzene 
• 459-57-4 4-fluorobenzaldehyde 
• 100-52-7 benzaldehyde 
• 61266-32-8 3-(4-nitrophenyl)prop-2-yn-1-ol 
• 5332-96-7 1-(4-nitrophenyl)propan-2-one 
• 74-99-7 prop-1-yne 

Downstream Products

• 2735-14-0 1,2-bis(4-nitrophenyl)acetylene 
• 503-17-3 dimethylacetylene 

Relevant articles and documents

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Regiospecific palladium-catalyzed cross-coupling reactions using the operational equivalent of 1,3-dilithiopropyne

A regiospecific palladium-catalyzed cross-coupling reaction using the operational equivalent of the dianion 1,3-dilithiopropyne, with aromatic iodides is reported. This reaction gives high yields of 1-propyn-1-yl-benzenes and 2-(propyn-1-yl)thiophenes in

Stereoselective Photoredox-Catalyzed Chlorotrifluoromethylation of Alkynes: Synthesis of Tetrasubstituted Alkenes

A new photoredox-catalyzed chlorotrifluoromethylation reaction of internal arylalkynes under mild conditions using visible light has been developed. The reactions proceed with high levels of regio- and stereoselectivity and utilize commercially available CF3SO2Cl as both the CF3 and Cl source. In the mechanistic pathway for this process, generation of the CF3 radical and chloride ion occurs by Ir(ppy)3-photocatalyzed reductive decomposition of CF3SO2Cl. The synthetically important trifluoromethyl-substituted vinyl chlorides produced in this process can be readily transformed to 1,1-bis-arylalkenes by using Suzuki coupling.