1356963-01-3

Basic information

• Product Name: 2-methoxy-5-methyl-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)aniline
• Synonyms: 2-methoxy-5-methyl-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)aniline
• CAS NO: 1356963-01-3
• Molecular Weight: 318.462
• Mol File: 1356963-01-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-methoxy-5-methyl-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-5-methyl-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)aniline(1356963-01-3)
• EPA Substance Registry System: 2-methoxy-5-methyl-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)aniline(1356963-01-3)

Safety Data

• Hazardous Substances Data: 1356963-01-3(Hazardous Substances Data)

Upstream product

• 1356963-00-2 1-(5-methoxy-2-methyl-4-nitrophenyl)piperidin-4-one 
• 1356962-93-0 8-(5-Methoxy-2-methyl-4-nitrophenyl)-1,4-dioxa-8-azaspiro[4.5]decane 
• 83341-28-0 5-fluoro-4-methyl-2-nitrophenol 
• 452-78-8 3-fluoro-4-methyl phenol 
• 1356962-90-7 1-(1-(5-methoxy-2-methyl-4-nitrophenyl)piperidin-4-yl)-4-methylpiperazine 
• 314298-13-0 1-fluoro-5-methoxy-2-methyl-4-nitro-benzene 
• 106579-00-4 5-methoxy-2-methyl-4-nitroaniline 

Relevant articles and documents

Novel(1,2,4)triazolo(1,5-a)pyridylphosphine oxide and use thereof

The present invention relates to novel(1,2,4)triazolo(1,5-a)pyridinyl phosphorus oxides and uses thereof. Wherein the compound is a compound represented by a formula I, or a pharmaceutically acceptable salt thereof, or a hydrate thereof, or a solvate thereof, or a metabolite thereof, or a stereoisomer thereof, or a tautomer thereof, or a prodrug thereof, and R1 to R5 are as defined in the specification. The compound disclosed by the invention can be used for preparing a medicine for treating and/or preventing cancers.

CHEMICAL COMPOUNDS

The present invention relates to compounds of Formula (I) and/or Formula (Ia): and to their salts, pharmaceutical compositions, methods of use, and methods for their preparation. These compounds inhibit ALK kinase activity, and thus may be used for the tr