872492-58-5

Basic information

• Product Name: (4-chloro-2-iodophenyl)methylamine
• Synonyms: (4-chloro-2-iodophenyl)methylamine
• CAS NO: 872492-58-5
• Molecular Weight: 267.497
• Mol File: 872492-58-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: (4-chloro-2-iodophenyl)methylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (4-chloro-2-iodophenyl)methylamine(872492-58-5)
• EPA Substance Registry System: (4-chloro-2-iodophenyl)methylamine(872492-58-5)

Safety Data

• Hazardous Substances Data: 872492-58-5(Hazardous Substances Data)

Upstream product

• 932-96-7 N-methyl(p-chloroaniline) 
• 1007-19-8 4-chloro-N-methyl-N-nitrosoaniline 
• 63069-48-7 p-chloro-o-iodoaniline 
• 74-88-4 methyl iodide 
• 942319-20-2 4-chloro-2-iodobenzamide 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 54960-76-8 2-chloro-5-methylphenanthridin-6(5H)-one 
• 1383543-75-6 C₁₅H₁₂ClN 
• 21261-85-8 6-chloro-3-methylbenzo[d]thiazole-2(3H)-thione 
• 60434-13-1 5-chloro-1-methylindoline-2, 3-dione 
• 62903-71-3 1-(5-chloro-2-(methylamino)phenyl)ethanone 
• 1609153-05-0 2-chloro-N-(4-chloro-2-iodophenyl)-N-methylacetamide 
• 63754-98-3 6-chloro-N-methyl-2(3H)-benzothiazolone 
• 1383675-31-7 4-chloro-2-iodo-N-methyl-N-(prop-2-ynyl)benzenamine 
• 1383675-47-5 1-benzyl-8-chloro-5-methyl-4,5-dihydro-1H-[1,2,3]triazolo[4,5-c]quinoline 
• 1220126-05-5 C₂₇H₂₁ClNPS 
• 1220125-92-7 5-chloro-2-(diphenylphosphinothioyl)-1-methyl-3-phenylindole 
• 872492-67-6 N-(4-chloro-2-iodophenyl)-N-methyl-1H-indole-2-carboxamide 
• 872492-62-1 N-(4-chloro-2-iodophenyl)-N-methyl-1H-pyrrole-2-carboxamide 

Relevant articles and documents

Accessing Unsymmetrically Linked Heterocycles through Stereoselective Palladium-Catalyzed Domino Cyclization

A palladium-catalyzed strategy is presented to synthesize unsymmetrically linked heterocycles within stereoselective tetrasubstituted olefins. This reaction is proposed to occur via a vinyl-PdII intermediate capable of initiating the cyclizatio

ACLY INHIBITORS AND USES THEREOF

The present invention provides compounds useful as inhibitors of ATP citrate lyase (ACLY), compositions thereof, and methods of using the same.

A catalyst-free and additive-free method for the synthesis of benzothiazolethiones from: O -iodoanilines, DMSO and potassium sulfide

Under catalyst-free and additive-free conditions, a novel, convenient, eco-friendly method for the synthesis of benzothiazolethiones has been developed. The three-component reaction of o-iodoanilines and K2S with DMSO proceeded smoothly and the corresponding benzothiazolethiones were obtained with good isolated yields. Meanwhile, this method could be used for the synthesis of thioureas from primary diamines. Furthermore, mechanism research showed that DMSO not only functioned as a carbon source, but also as a mild oxidant in this reaction.