209688-45-9

Basic information

• Product Name: 4-methoxycarbonylphenyl 5-chloro-2-aminobenzyl ether
• Synonyms: 4-methoxycarbonylphenyl 5-chloro-2-aminobenzyl ether
• CAS NO: 209688-45-9
• Molecular Weight: 291.734
• Mol File: 209688-45-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-methoxycarbonylphenyl 5-chloro-2-aminobenzyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxycarbonylphenyl 5-chloro-2-aminobenzyl ether(209688-45-9)
• EPA Substance Registry System: 4-methoxycarbonylphenyl 5-chloro-2-aminobenzyl ether(209688-45-9)

Safety Data

• Hazardous Substances Data: 209688-45-9(Hazardous Substances Data)

Upstream product

• 209688-14-2 methyl 4-[(5-chloro-2-nitrobenzyl)oxy]benzoate 
• 7439-89-6 iron 
• 209688-13-1 5-chloro-2-nitrobenzyl methanesulfonate 
• 73033-58-6 5-chloro-2-nitrobenzyl alcohol 
• 6628-86-0 5-chloro-2-nitrobenzaldehyde 

Downstream Products

• 209685-41-6 methyl 4-[(5-chloro-2-{[(4-chlorophenyl)sulfonyl]amino}benzyl)oxy]benzoate 

Relevant articles and documents

Chemoselective hydrogenation of nitrobenzyl ethers to aminobenzyl ethers catalyzed by palladium-nickel bimetallic nanoparticles

A highly efficient and chemoselective hydrogenation of nitrobenzyl ethers to aminobenzyl ethers was developed by using a novel palladium-nickel bimetallic nanocatalyst. Since the catalytic selectivity was resulted from the synergistic effects between two metals rather than the traditional catalyst poisons, the hydrogenation proceeded smoothly under additive-free conditions. Thus, the work-up procedure was as simple as to recover the catalyst by a magnetic separation and then to evaporate the solvent.

Sulfonamide and carboxamide derivatives and drugs containing the same as the active ingredient

The sulfonamide or carboamide derivatives of the formula (I) and a pharmaceutical composition which comprise them as an active ingredient: (wherein A ring, B ring is carbocyclic ring, heterocyclic ring; Z1is —COR1, —CH═CH—COR1/