10342-62-8

Basic information

• Product Name: Ethanone, 1-(2-nitrophenyl)-, oxime
• CAS NO: 10342-62-8
• Molecular Formula: C8H8N2O3
• Molecular Weight: 180.163
• Mol File: 10342-62-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(2-nitrophenyl)-, oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2-nitrophenyl)-, oxime(10342-62-8)
• EPA Substance Registry System: Ethanone, 1-(2-nitrophenyl)-, oxime(10342-62-8)

Safety Data

• Hazardous Substances Data: 10342-62-8(Hazardous Substances Data)

Upstream product

• 540-80-7 tert.-butylnitrite 
• 612-22-6 2-nitro(ethylbenzene) 
• 110-46-3 isopentyl nitrite 
• 577-59-3 2-acetylnitrobenzene 

Downstream Products

• 109963-56-6 1-(2-nitro-phenyl)-ethanone-((E)-O-picryl oxime ) 
• 577-59-3 2-acetylnitrobenzene 
• 552-32-9 o-nitroacetanilide 
• 39909-26-7 2-(1-aminoethyl)aniline 
• 126267-63-8 2-(2-nitro-phenyl)-imidazo[1,2-a]pyridine 
• 1463-62-3 1-(2-nitro-phenyl)-ethanone-(2,4-dinitro-phenylhydrazone) 
• 3176-62-3 3-methyl-1H-indazole 
• 551-93-9 2-aminoacetophenone 

Relevant articles and documents

Electrophilically activated nitroalkanes in synthesis of 3,4-dihydroquinozalines

Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various heterocycles. This strategy was employed to develop an innovative synthetic approach towards 3,4-dihydroquinazolines from readily available 2-(aminomethyl)anilines.

Preparation method of pyrimidine salicylate oxime ester compound and application of compound as herbicide

The invention discloses a preparation method of a pyrimidine salicylate oxime ester compound and application of the compound as a herbicide, belongs to the technical field of herbicides, and relates to the application of the herbicide in selectively controlling gramineous weeds and broadleaf weeds for crops. The compound is a pyrithiobac oxime ester compound. The preparation method includes the following steps that acids of pyrithiobac are condensed with substituted acetophenoxime in the presence of an organic solvent and a condensation agent to prepare a (I) compound. At 45 g a.i./hm, thecompound can effectively control echinochloa crusgalli, eleusineindica, setaria viridis, amaranthus retroflexus, portulaca oleracea, chenopodium album and other grassy weeds and broadleaf weeds, can serve as a candidate herbicide in a cotton field and has potential industrial application. Meanwhile, the compound is environmentally friendly, low in toxicity and highly safe for crops such as cotton.The invention provides a preparation technology of the efficient and safe novel pyrimidine salicylate oxime ester compound with the herbicidal activity, the compound can be massively produced, the yield is high and the purity is high.