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

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

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.

Cp?Rh(iii) catalyzed: Ortho -halogenation of N -nitrosoanilines by solvent-controlled regioselective C-H functionalization

We present a novel, efficient, and regioselective method for the rhodium-catalyzed direct C-H ortho-halogenation of anilines that involves a removable N-nitroso directing group. This method featured mild reaction conditions, wide substrate scope, good functional group tolerance and satisfactory yields. To maintain the high ortho-regioselectivity and conversion, increasing the steric hindrance of the solvent was critical. Preliminary mechanistic studies suggest that C-H activation may be involved in the rate-determining step.