52287-58-8

Basic information

• Product Name: (E)-2,4-dichloro-1-(2-nitroprop-1-en-1-yl)benzene
• Synonyms: (E)-2,4-dichloro-1-(2-nitroprop-1-en-1-yl)benzene
• CAS NO: 52287-58-8
• Molecular Weight: 232.066
• Mol File: 52287-58-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: (E)-2,4-dichloro-1-(2-nitroprop-1-en-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2,4-dichloro-1-(2-nitroprop-1-en-1-yl)benzene(52287-58-8)
• EPA Substance Registry System: (E)-2,4-dichloro-1-(2-nitroprop-1-en-1-yl)benzene(52287-58-8)

Safety Data

• Hazardous Substances Data: 52287-58-8(Hazardous Substances Data)

Upstream product

• 79-24-3 Nitroethane 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 960053-43-4 C₉H₉Cl₂NO₃ 
• 75-52-5 nitromethane 

Downstream Products

• 4380-31-8 [2-bromo-1-(2,4-dichloro-phenyl)-2-nitro-propyl]-methyl ether 
• 951017-42-8 N-[2-(2,4-dichlorophenyl)-1-methylethyl]-2-trifluoromethylpyrazine-3-carboxamide 
• 951017-41-7 N-[2-(2,4-dichloro-phenyl)-1-methylethyl]-2-trifluoromethylbenzamide 
• 78874-19-8 2-(2,4-dichlorophenyl)-3-methylquinoxaline 
• 1442645-58-0 C₂₀H₁₇Cl₂NO₂ 
• 1426080-01-4 2-(2,4-dichlorophenyl)-3-methylimidazo[1,2-a]pyridine 
• 1374229-54-5 1-[4-(2,4-dichlorophenyl)-2,5-dimethylfuran-3-yl]ethanone 
• 95838-60-1 4-(2,4-Dichlorphenyl)-2,5-dimethyl-3-pyrrolcarbonsaeure-methylester 
• 1374229-55-6 ethyl 4-(2,4-dichlorophenyl)-2,5-dimethylfuran-3-carboxylate 
• 1320232-30-1 C₂₀H₁₇Cl₂NO₂ 
• 1092400-97-9 2,4-dichloro-1-(1-methoxy-2-nitro-propyl)-benzene 
• 1092400-99-1 N-[1-(2,4-dichloro-phenyl)-2-nitro-propyl]-O-methyl-hydroxylamine 
• 32560-77-3 2-(2,4-dichloro-phenyl)-1-methyl-ethylamine 
• 89730-49-4 5-<(Acetyl)(methoxycarbonyl)methylenamino>-4-(2,4-dichlorphenyl)-4,5-dihydro-2,5-dimethyl-3-furancarbonsaeure-methylester 

Relevant articles and documents

Iron-catalyzed tandem one-pot addition and cyclization of the blaise reaction intermediate and nitroolefins: Synthesis of substituted NH-pyrroles from nitriles

The iron-catalyzed addition and cyclization of the Blaise reaction intermediate and nitroolefins to synthesize highly functionalized NH-pyrroles in a tandem one-pot manner from nitriles has been developed. This reaction shows good functional group tolerance and affords a broad spectrum of substituted NH-pyrroles in good yields. Copyright

Ethylenediamine: A highly effective catalyst for one-pot synthesis of aryl nitroalkenes via henry reaction and dehydration

Ethylenediamine (H2NCH2CH2NH2) was found to be a highly effective catalyst for the condensation of aryl aldehydes with nitromethane (or nitroethane). When 1%-2% (mol%) of ethylenediamine was used as the catalyst, the one-pot reaction of aryl aldehydes with nitromethane (or nitroethane) by refluxing for 3-10 h efficiently afforded various arylnitroalkenes 1a-1y in 85%-97% yields. Ethylenediamine (H 2NCH2CH2NH2) was found to be a highly effective catalyst for the condensation of aryl aldehydes with nitromethane (or nitroethane). When 1-2 mol% of ethylenediamine was used as the catalyst, the one-pot reaction of aryl aldehydes with nitromethane (or nitroethane) by refluxing for 3-10 h efficiently afforded various aryl nitroalkenes 1a-1y in 85%-97% yields. Copyright

NOVEL MICROBIOCIDES

Compounds of formula (I) in which the substituents are as defined in claim 1,are suitable for use as microbiocides.