111453-03-3

Basic information

• Product Name: Benzenesulfonamide, 4-methyl-N-[4-[(4-nitrophenyl)thio]phenyl]-
• CAS NO: 111453-03-3
• Molecular Formula: C19H16N2O4S2
• Molecular Weight: 400.479
• Mol File: 111453-03-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-[4-[(4-nitrophenyl)thio]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-[4-[(4-nitrophenyl)thio]phenyl]-(111453-03-3)
• EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-[4-[(4-nitrophenyl)thio]phenyl]-(111453-03-3)

Safety Data

• Hazardous Substances Data: 111453-03-3(Hazardous Substances Data)

Upstream product

• 101-59-7 4-amino-4'-nitrodiphenyl sulfide 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 857005-70-0 toluene-4-sulfonic acid-[N-isopropyl-4-(4-nitro-phenylsulfanyl)-anilide] 
• 857004-46-7 toluene-4-sulfonic acid-[N-butyl-4-(4-nitro-phenylsulfanyl)-anilide] 
• 874514-18-8 toluene-4-sulfonic acid-[4-(4-nitro-benzenesulfonyl)-N-octyl-anilide] 
• 857004-76-3 toluene-4-sulfonic acid-[N-allyl-4-(4-nitro-phenylsulfanyl)-anilide] 
• 857004-42-3 toluene-4-sulfonic acid-[N-sec-butyl-4-(4-nitro-phenylsulfanyl)-anilide] 
• 859491-37-5 toluene-4-sulfonic acid-[N-hexadecyl-4-(4-nitro-benzenesulfonyl)-anilide] 
• 859495-71-9 toluene-4-sulfonic acid-[N-(4-nitro-benzyl)-4-(4-nitro-phenylsulfanyl)-anilide] 
• 859492-61-8 toluene-4-sulfonic acid-[N-(2,3-dihydroxy-propyl)-4-(4-nitro-phenylsulfanyl)-anilide] 
• 176512-29-1 4-(N-propyl-N-tosyl)-amino-4'-nitrodiphenyl sulfide 
• 858254-22-5 N-[4-(4-nitro-phenylsulfanyl)-phenyl]-N-(toluene-4-sulfonyl)-glycine ethyl ester 
• 854859-36-2 2-[4-(4-nitro-phenylsulfanyl)-N-(toluene-4-sulfonyl)-anilino]-butyric acid ethyl ester 
• 111453-06-6 4--4'-nitrodiphenylsulphide 
• 859491-22-8 toluene-4-sulfonic acid-(N-hexadecyl-4-sulfanilyl-anilide) 
• 859495-78-6 toluene-4-sulfonic acid-[4-(4-nitro-benzenesulfonyl)-N-(4-nitro-benzyl)-anilide] 

Relevant articles and documents

The iridium-catalyzed synthesis of symmetrically and unsymmetrically alkylated diamines under mild reaction conditions

An iridium catalyst - stabilized by an anionic P,N ligand - was used for the symmetrical and unsymmetrical monoalkylation of para-, meta-, and ortho-benzenediamines. Benzyl and aliphatic alcohols were used as alkylating reagents. 28 derivatives were synthesized. 14 of them are new compounds. Furthermore, the alkylation of the pharmacological important diamine Dapson (dapsone) is described. 14 dapsone derivatives were synthesized among them 9 new compounds. Copyright

Diaryl sulphide derivatives

A diaryl sulphide derivative of the formula STR1 in which R1 represents a thiazolamino radical of the formulae STR2 wherein R5 represents hydrogen, alkyl, aralkyl or acyl, R6 and R6 ' are identical or different