4094-39-7

Basic information

• Product Name: N-{4-[(4-methylphenyl)sulfonyl]phenyl}acetamide
• Synonyms: acetamide, N-[4-[(4-methylphenyl)sulfonyl]phenyl]-; N-{4-[(4-Methylphenyl)sulfonyl]phenyl}acetamide
• CAS NO: 4094-39-7
• Molecular Formula: C₁₅H₁₅NO₃S
• Molecular Weight: 289.3495
• Mol File: 4094-39-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 530.2°C at 760 mmHg
• Flash Point: 274.5°C
• Density: 1.273g/cm³
• Vapor Pressure: 2.51E-11mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: N-{4-[(4-methylphenyl)sulfonyl]phenyl}acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-{4-[(4-methylphenyl)sulfonyl]phenyl}acetamide(4094-39-7)
• EPA Substance Registry System: N-{4-[(4-methylphenyl)sulfonyl]phenyl}acetamide(4094-39-7)

Safety Data

• Hazardous Substances Data: 4094-39-7(Hazardous Substances Data)

Upstream product

• 339096-10-5 N-[4-(p-tolylthio)phenyl]acetamide 
• 121-60-8 p-acetylaminobenzenesulfonyl chloride 
• 622-50-4 4-Acetamido-1-iodobenzene 
• 418767-54-1 (+/-)-4-(acetamino)phenyl 4-methylphenyl sulfoxide 
• 536-57-2 p-toluene sulfinic acid 
• 51176-55-7 (+/-)-4-aminophenyl 4-methylphenyl sulfoxide 
• 62-53-3 aniline 
• 101251-09-6 (4-acetylaminophenyl)boronic acid 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Downstream Products

• 4094-38-6 4-aminophenyl 4-methylphenyl sulfone 

Relevant articles and documents

Catalyst-free arylation of sulfonamidesviavisible light-mediated deamination

A novel arylation of sulfonamides with boronic acids to afford numerous diaryl sulfonesviaa visible light-mediated N-S bond cleavage other than the typical transition-metal-catalyzed C(O)-N bond activation is described. This methodology, which represents the first catalyst-free protocol for the sulfonylation of boronic acids, is characterized by its simple reaction conditions, good functional group tolerance and high efficiency. Several successful examples for the late-stage functionalization of diverse sulfonamides indicate the high potential utility of this method in pharmaceutical science and organic synthesis.

Syntheses, absolute configurations, and UV/Vis spectroscopic properties of new chiral tri- and pentamethinium streptocyanine dyes with 4-aminophenyl 4-methylphenyl sulfoxide endgroups

Starting with monochiral 4-aminophenyl 4-methylphenyl sulfoxides 3a and 3b, the absolute configurations of which were determined by X-ray analysis, we have synthesized the new chiral C2-symmetrical tri- and pentamethinium streptocyanine dyes 5a