74205-57-5

Upstream product

• 109-65-9 1-bromo-butane 
• 25263-44-9 3-Hydroxyphenylacetonitrile 
• 19924-43-7 3-methoxyphenylacetonitrile 
• 620-24-6 3-Hydroxybenzyl alcohol 
• 151-50-8 potassium cyanide 
• 99047-07-1 m-butoxybenzyl chloride 
• 30609-21-3 (3-butoxyphenyl)methanol 

Downstream Products

• 74316-87-3 1-(3-Butoxy-phenyl)-cyclopentanecarbonitrile 
• 89790-03-4 m-butoxyphenylacetamide 
• 74205-05-3 1-(3-Butoxy-phenyl)-cyclopropanecarbonitrile 
• 74205-19-9 1-(3-Butoxy-phenyl)-cyclobutanecarbonitrile 
• 74205-33-7 1-(3-Butoxy-phenyl)-cyclopropanecarboxylic acid 
• 74205-47-3 1-(3-Butoxy-phenyl)-cyclobutanecarboxylic acid 
• 74316-94-2 1-(3-butoxy-phenyl)-cyclopentanecarboxylic acid 
• 61492-26-0 (2S,5R,6R)-6-{[1-(3-Butoxy-phenyl)-cyclopropanecarbonyl]-amino}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 61492-42-0 (2S,5R,6R)-6-{[1-(3-Butoxy-phenyl)-cyclobutanecarbonyl]-amino}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 61492-11-3 (2S,5R,6R)-6-{[1-(3-Butoxy-phenyl)-cyclopentanecarbonyl]-amino}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 1417442-64-8 2,2-difluoro-2-(3-butoxyphenyl)ethylamine 
• 1417442-65-9 N-(tert-butoxycarbonyl)-2,2-difluoro-2-(3-butoxyphenyl)ethylamine 
• 1417442-66-0 2-[N-(tert-butoxycarbonyl)-2,2-difluoro-2-(3-butoxyphenyl)-ethylamino]-N,N-dimethyl-acetamide 
• 1417442-67-1 2-[N-tert-butoxycarbonyl-2,2-difluoro-2-(3-butoxyphenyl)-ethylamino]-N,N-dimethylpropanamide 

Relevant academic research and scientific papers

FLUORINATED ARYLALKYLAMINOCARBOXAMIDE DERIVATIVES

Fluorinated arylalkylaminocarboxamide derivatives of formula (I) are described wherein W, J, n, R1, R2, R3, R4, R5 and R6 have the meanings as defined in the specification and pharmaceutica

FLUORINATED ARYLALKYLAMINOCARBOXAMIDE DERIVATIVES

Fluorinated arylalkylaminocarboxamide derivatives of formula (I) are described wherein W, J, n, R1, R2, R2', R3, R4, R5 and R6 have the meanings as defined in the specification a

Nitrogen containing heterocyclic compounds

Compounds of the formula (III): STR1 or salts or acyl derivatives thereof, for use as antifungal and antiprotozoal agents are disclosed. Compositions containing the compounds are also disclosed as are method for the preparation of the compounds and interm

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.