90544-88-0

Upstream product

• 67-56-1 methanol 
• 619-91-0 2-[(4-nitrophenyl)amino]acetic acid 

Downstream Products

• 1312021-86-5 C₁₇H₁₂F₃N₃O₅ 
• 1181215-05-3 [(2-chloroacetyl)-(4-trifluoromethoxyphenyl)amino]acetic acid methyl ester. 
• 851680-25-6 [(4-(Bismethanesulfonyl)amino-phenyl)-(2,2,2-trifluoro-acetyl)-amino]-acetic acid methyl ester 
• 851680-24-5 [(4-Amino-phenyl)-(2,2,2-trifluoro-acetyl)-amino]-acetic acid methyl ester 
• 851680-27-8 N-4-propanesulfonylamino-phenylglycine 
• 773844-67-0 N-4-methanesulfonylamino-phenylglycine 
• 851680-23-4 [(4-Nitro-phenyl)-(2,2,2-trifluoro-acetyl)-amino]-acetic acid methyl ester 

Relevant academic research and scientific papers

Microwave-assisted deformylation of N-aryl formamide by KF on basic Al2O3

The formyl group was successfully removed from N-aryl formamide by KF on a solid support of basic Al2O3 in 4-20 min with microwave irradiation. The conditions mimic base-catalyzed hydrolysis of formamide and are compatible with carbamates and t-butyl esters, but not methyl, ethyl, and benzyl esters.

Novel phenylamino acetamide derivatives as potent and selective κ opioid receptor agonists

A novel series of phenylamino acetamide derivatives was synthesized. These amides were shown to be potent and selective κ opioid receptor agonists.

Amide derivatives and methods of their use

Amide derivatives of the general formulae Ia and Ib: are disclosed. Pharmaceutical compositions containing these compounds, and methods for their use, inter alia, for treating and/or preventing gastrointestinal disorders, pain, and pruritus are also disclosed.