18982-43-9

Usage

Uses

Used in Pharmaceutical Synthesis:
1-(2-Chlorophenyl)-2-nitropropene is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows for the development of new medications with specific therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 1-(2-Chlorophenyl)-2-nitropropene is utilized as a starting material for the creation of different agrochemicals, such as pesticides and herbicides. Its chemical properties make it a valuable component in the development of these products.
Used in Fine Chemicals Manufacturing:
1-(2-Chlorophenyl)-2-nitropropene is also employed in the production of fine chemicals, which are high-purity chemicals used in various applications, including research, diagnostics, and specialty manufacturing processes.
Used as an Intermediate in Organic Synthesis:
1-(2-CHLOROPHENYL)-2-NITROPROPENE serves as an intermediate in organic synthesis, where it can be converted into other useful compounds for a wide range of applications across different industries. Its versatility in chemical reactions makes it a valuable asset in the field of organic chemistry.

InChI:InChI=1/C9H8ClNO2/c1-7(11(12)13)6-8-4-2-3-5-9(8)10/h2-6H,1H3/b7-6+

Upstream product

• 79-24-3 Nitroethane 
• 89-97-4 2-CHLOROBENZYLAMINE 
• 89-98-5 2-chloro-benzaldehyde 

Downstream Products

• 91473-99-3 5-<(Acetyl)(tert-butoxycarbonyl)methylenamino>-4-(2-chlorphenyl)-4,5-dihydro-2,5-dimethyl-3-furancarbonsaeure-tert-butylester 
• 126760-75-6 3-(2-Chloro-phenyl)-4-methyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 1723-25-7 ethyl 2,3-dioxobutyrate 
• 95838-65-6 4-(2-Chlorphenyl)-2,5-dimethyl-3-pyrrolcarbonsaeure-ethylester 
• 95838-90-7 5-<(Acetyl)(methoxycarbonyl)methylenamino>-4-(2-chlorphenyl)-4,5-dihydro-2,5-dimethyl-3-furancarbonsaeure-methylester 
• 109703-84-6 2-<4-Benzoyl-3-(2-chlorphenyl)-2,3-dihydro-2-methyl-5-phenyl-2-furylimino>-1,3-diphenyl-1,3-propandion 
• 4435-51-2 1-phenyl-butane-1,2,3-trione 
• 109703-96-0 <4-(2-Chlorphenyl)-2,5-dimethyl-3-pyrrolyl>phenylketon 
• 109703-78-8 2-<4-Benzoyl-3-(2-chlorphenyl)-2,3-dihydro-2,5-dimethyl-3-phenyl-2-furylimino>-1-phenyl-1,3-butandion 
• 109704-00-9 <4-(2-Chlorphenyl)-5-methyl-2-phenyl-3-pyrrolyl>phenylketon 
• 109735-35-5 <1-(1-Benzoyl-2-hydroxy-2-phenylvinyl)-4-(2-chlorphenyl)-5-methyl-2-phenyl-3-pyrrolyl>phenylketon 
• 858220-11-8 N-hydroxy-1-methyl-2-(2-chlorophenyl)ethanamine 
• 1374229-53-4 ethyl 4-(2-chlorophenyl)-2,5-dimethylfuran-3-carboxylate 
• 95838-58-7 4-(2-Chlorphenyl)-2,5-dimethyl-3-pyrrolcarbonsaeure-methylester 

Relevant academic research and scientific papers

Substrate promiscuity of ortho-naphthoquinone catalyst: Catalytic aerobic amine oxidation protocols to deaminative cross-coupling and n-nitrosation

ortho-Naphthoquinone-based organocatalysts have been identified as versatile aerobic oxidation catalysts. Primary amines were readily cross-coupled with primary nitroalkanes via deaminative pathway to give nitroalkene derivatives in good to excellent yields. Secondary and tertiary amines were inert to ortho-naphthoquinone catalysts; however, secondary nitroalkanes were readily converted by ortho-naphthoquinone catalysts to the corresponding nitrite species that in situ oxidized the amines to the corresponding N-nitroso compounds. Without using harsh oxidants in a stoichiometric amount, the present catalytic aerobic oxidation protocol utilizes the substrate promiscuity feature to provide a facile access to amine oxidation products under mild reaction conditions.

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

An efficient solventless synthesis of α-aryl-N-[1-methyl-2-(2/4- chlorophenyl)] ethyl nitrones and their antimicrobial activity

An efficient solventless synthesis of α-aryl-N-[1-methyl-2-(2/4- chlorophenyl)]ethyl nitrones has been achieved in excellent yield. The compounds are characterized by NMR and X-ray studies. The antimicrobial activities of the synthesized compounds have al

Porphyrin synthesis from nitrocompounds

A new porphyrin synthesis starting from nitroalkenes or their equivalents is described. For example, octaethylporphyrin, coproporphyrin, porphyrin-1,2,3,4,5,6,7,8 octapropionic acid, and 2,7,12,17 tetraarylporphyrin are prepared in good yield from readily available materials such as 1-nitropropane, nitroethane, nitromethane, and aldehydes.