26288-57-3

Basic information

• Product Name: 1H-Pyrrole, 3-(4-chlorophenyl)-
• CAS NO: 26288-57-3
• Molecular Formula: C10H8ClN
• Molecular Weight: 177.633
• Mol File: 26288-57-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole, 3-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole, 3-(4-chlorophenyl)-(26288-57-3)
• EPA Substance Registry System: 1H-Pyrrole, 3-(4-chlorophenyl)-(26288-57-3)

Safety Data

• Hazardous Substances Data: 26288-57-3(Hazardous Substances Data)

Upstream product

• 106-39-8 bromochlorobenzene 
• 7560-44-3 methyl 4-chlorocinnamate 
• 76304-28-4 dimethyl 3-(4-chlorophenyl)-1H-pyrrole-2,4-dicarboxylate 
• 68001-86-5 methyl (Z)-3-(4-chlorophenyl)-2-isocyanoacrylate 
• 68185-82-0 (E)-3-(4-Chloro-phenyl)-2-isocyano-acrylic acid methyl ester 
• 20754-21-6 methyl 3-(4-chlorophenyl)propenoate 
• 1073-67-2 4-vinylbenzyl chloride 
• 38622-91-2 [(p-methylphenyl)sulfonylmethyl]isonitrile 
• 122453-98-9 4-(4-Chloro-phenyl)-1H-pyrrole-3-carboxylic acid 
• 138900-61-5 1-(triisopropylsilyl)-3-(4-chlorophenyl)pyrrole 

Downstream Products

• 1345502-19-3 C₁₅H₁₇ClN₂O₂ 

Relevant articles and documents

One-step synthesis of 3-aryl- and 3,4-diaryl-(1H)-pyrroles using tosylmethyl isocyanide (TOSMIC)

(matrix presented) A one-step synthesis of 3-aryl and 3,4-diaryl-(1H)-pyrroles from TOSMIC and commercially available or readily synthesized arylalkenes is reported. Optimal conditions were found to be NaOtBu in DMSO. The methodology was particularly efficient (yields > 65%) when electron poor aryl groups were attached to the alkene.

An efficient method for the synthesis of 3-arylpyrroles

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Arylpyrrole insecticidal acaricidal and nematicidal agents and methods for the preparation thereof

This invention is directed to certain novel insecticidal, acaricidal and nematicidal arylpyrrole agents and a method for controlling insects, acarids and nematodes therewith. The invention also is directed to a method for protecting growing plants from insect, acarid and nematode attack by applying to said plants or the soil in which they are growing, an insecticidally, acaricidally or nematicidally effective amount of a novel arylpyrrole compound. The present invention further is directed to a method for the preparation of the arylpyrrole compounds.