3559-06-6

Usage

Sulfonate group

Attached to a 4-methylbenzene ring The sulfonate group (-SO3H) is a key functional group in 2-{methyl[(4-methylphenyl)sulfonyl]amino}ethyl 4-methylbenzenesulfonate, providing acidic properties and opportunities for reactions with other chemicals.

Secondary amine group

Connected to an ethyl chain The amine group (-NH2) in 2-{methyl[(4-methylphenyl)sulfonyl]amino}ethyl 4-methylbenzenesulfonate is secondary, meaning it is attached to two carbon atoms, one of which is part of an ethyl chain (-CH2-).

Methylsulfonylphenyl group

Part of the amine group The amine group is connected to a methylsulfonylphenyl group, which adds further complexity and potential reactivity to the compound.

Applications in pharmaceutical or chemical industries

Potentially used as a reagent, intermediate, or precursor Due to its complex structure and functional groups, this chemical may be used in the synthesis of other organic compounds or as a component in pharmaceutical products.

Specific uses in organic synthesis

The presence of various functional groups suggests that 2-{methyl[(4-methylphenyl)sulfonyl]amino}ethyl 4-methylbenzenesulfonate may have unique applications in organic synthesis, such as catalyzing reactions or acting as a building block for more complex molecules.

Component in pharmaceutical products

The complex structure of the compound may make it suitable for use in pharmaceutical products, either as an active ingredient or as a辅助成分 to improve the properties of the final product.

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 109-83-1 (2-hydroxyethyl)(methyl)amine 

Downstream Products

• 3409-85-6 N-Methyl-N-(4-toluenesulphonyl)iodoethylamine 
• 1146480-74-1 N-{2-[1-(2-methoxy-phenyl)-4-oxo-3H-pyrido[3,4-d]pyridazin-3-yl]-ethyl}-4,N-dimethyl-benzenesulfonamide 
• 1146480-72-9 N,4-dimethyl-N-[2-((1-oxo-1H-phthalazin-2)-yl)ethyl]benzenesulfonamide 
• 912346-05-5 N-{2-[(3S,4R,5R)-4-[4-((S)-3-methoxy-2-methylpropoxymethyl)phenyl]-5-[4-(3-methoxypropyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-1-(toluene-4-sulphonyl)-piperidin-3-yloxy]ethyl}-N-methylbenzenesulphonamide 
• 911210-71-4 N-{2-[5-[4-(3-methoxypropyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-4-[4-(4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-yloxy)phenyl]-1-(toluene-4-sulphonyl)piperidin-3-yloxy]ethyl}-4,N-dimethylbenzenesulphonamide 
• 141766-07-6 1,16-Ditosyl-1,4,7,10,13,16-hexamethylpentaethylenehexamine 
• 141766-06-5 1,13-Ditosyl-1,4,7,10,13-pentamethyltetramethylenepentamine 
• 141766-05-4 1,10-Ditosyl-1,4,7,10-tetramethyltriethylenetetramine 
• 141766-04-3 1,4,7-trimethyl-1,7-bis(p-tolylsulfonyl)-1,4,7-triazaheptane 

Relevant academic research and scientific papers

XANTHENE COMPOUND AND COLORING COMPOSITION

PROBLEM TO BE SOLVED: To provide a xanthene compound having good brightness and excellent fastness such as heat resistance, and a coloring composition thereof. SOLUTION: A xanthene compound is represented by the formula (1) (where, R1 and Rsup

Substituted Piperidines as Renin Inhibitors

Compounds of the general formula (I) in which the meanings of the substituents R1, R2, R3, R4, X, Z and n as stated in claim 1 have renin-inhibiting properties and can be used as medicines.

Substituted piperidines as therapeutic compounds

Use of compounds of the general formula (1) and pharmaceutically acceptable salt thereof, in which R1, R2, R3, R4, W, X, Z and n have the definitions illustrated in detail in the description, as beta-secretase, cathepsin D, plasmepsin II and/or HIV protease inhibitors.

SUBSTITUTED PIPERIDINES AS RENIN INHIBITORS

Compounds of the general formula (I) in which the meanings of the substituents R1, R2, R3, R4, W, X, Z and n as stated in Claim 1 have renin-inhibiting properties and can be used as medicines.