10285-90-2

Basic information

• Product Name: N-butyl-4-methyl-N-[(4-methylphenyl)sulfonyl]benzenesulfonamide
• CAS NO: 10285-90-2
• Molecular Formula: C₁₈H₂₃NO₄S₂
• Molecular Weight: 381.5095
• Mol File: 10285-90-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 521.5°C at 760 mmHg
• Flash Point: 269.2°C
• Density: 1.243g/cm³
• Vapor Pressure: 5.64E-11mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: N-butyl-4-methyl-N-[(4-methylphenyl)sulfonyl]benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-butyl-4-methyl-N-[(4-methylphenyl)sulfonyl]benzenesulfonamide(10285-90-2)
• EPA Substance Registry System: N-butyl-4-methyl-N-[(4-methylphenyl)sulfonyl]benzenesulfonamide(10285-90-2)

Safety Data

• Hazardous Substances Data: 10285-90-2(Hazardous Substances Data)

Upstream product

• 109-73-9 N-butylamine 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Nickel-catalyzed one-pot Suzuki-Miyaura cross-coupling of phenols and arylboronic acids mediated by N,N-ditosylaniline

An efficient method for the construction of two distinct C aryl-Caryl bonds through the Ni-catalyzed Suzuki-Miyaura cross-coupling of phenols with arylboronic acids has been developed. This reaction proceeds through the in situ tosylation of phenols by using N,N-ditosylaniline as the sulfonylating reagent, which is highly active, markedly stable, and easily prepared. The scope with respect to the coupling partners - phenols and boronic acids - is broad, and sensitive functional groups are tolerated. Phenols, especially those containing an unprotected amino group, which are generally problematic for coupling under conventional one-pot conditions, are also viable substrates in this transformation.

Infrared spectra of bisarylsulfonimide derivatives

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