99758-66-4

Upstream product

• 85943-26-6 5-tert-butyl-2-methoxybenzaldehyde 
• 5396-38-3 1-(tert-butyl)-4-methoxybenzene 
• 85943-75-5 5-tert-butyl-2-hydroxy-3-nitrobenzaldehyde 
• 77-78-1 dimethyl sulfate 
• 2725-53-3 2-hydroxy-5-t-butylbenzaldehyde 
• 22252-73-9 2-chloromethyl-4-tert-butylanisole 

Downstream Products

• 848144-43-4 5-(tert-butyl)-2-methoxy-3-nitrobenzoic acid 
• 1269761-63-8 C₂₄H₃₂N₂O₃ 
• 1269761-67-2 C₃₆H₄₇N₃O₄ 
• 1269761-68-3 C₄₈H₆₂N₄O₅ 
• 1269761-69-4 C₆₀H₇₇N₅O₆ 
• 1269761-70-7 C₇₂H₉₂N₆O₇ 
• 1269761-71-8 C₈₄H₁₀₇N₇O₈ 
• 1215031-67-6 5-tert-butyl-2-methoxy-1-methylsulphanylmethyl-3-nitro-benzene 
• 1215031-68-7 5-tert-butyl-2-methoxy-3-nitro-benzyl methanesulphonate 
• 1283526-70-4 5-tert-butyl-2-methoxy-3-(2,2,2-trifluoro-1-(methylamino)ethyl)aniline 
• 1283526-67-9 1-(5-tert-butyl-2-methoxy-3-nitrophenyl)-2,2,2-trifluoro-N-methylethaneamine 
• 1283526-66-8 1-(5-tert-butyl-2-methoxy-3-nitrophenyl)-2,2,2-trifluoroethanone 
• 1283526-63-5 tert-butyl 1-(5-tert-butyl-2-methoxy-3-nitrophenyl)-2,2,2-trifluoroethylcarbamate 
• 1283525-70-1 1-(5-tert-butyl-2-methoxy-3-((S)-2,2,2-trifluoro-1-hydroxyethyl)phenyl)-3-((1S,2R)-1-hydroxy-2,3-dihydro-1H-indene-2-yl)urea 

Relevant academic research and scientific papers

NOVEL BENZAMIDES, PRODUCTION THEREOF, AND USE THEREOF AS MEDICAMENTS

Heteroaryloxy-substituted benzoic acid amides of general formula I wherein the groups R1 to R7 as well as X and Y are defined according to claim 1, including the tautomers, the stereoisomers, the mixtures and the salts thereof. The compounds according to the invention are suitable for the treatment of respiratory complaints, particularly COPD and asthma.

7-(Piperazine-1-Ymethyl)-1H-Indole-2-Carboxylic Acid (Phenyl)-Amide Derivatives and Allied Compounds as P38 Map Kinase Inhibitors for the Treatment of Respiratory Diseases

The present invention provides compounds according to general formula (I) which are proposed for the treatment of respiratory complaints, particularly asthma and COPD.

Campestarenes: Novel shape-persistent Schiff base macrocycles with 5-fold symmetry

A simple 1-step procedure yields a family of easily modifiable, stable, conjugated Schiff base macrocycles with 5-fold symmetry mediated by 3-center hydrogen bonding.