73424-46-1

Basic information

• Product Name: N-(2,3-dihydroinden-1-ylideneamino)-4-methyl-benzenesulfonamide
• CAS NO: 73424-46-1
• Molecular Formula: C₁₆H₁₆N₂O₂S
• Molecular Weight: 300.381
• Mol File: 73424-46-1.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: N-(2,3-dihydroinden-1-ylideneamino)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,3-dihydroinden-1-ylideneamino)-4-methyl-benzenesulfonamide(73424-46-1)
• EPA Substance Registry System: N-(2,3-dihydroinden-1-ylideneamino)-4-methyl-benzenesulfonamide(73424-46-1)

Safety Data

• Hazardous Substances Data: 73424-46-1(Hazardous Substances Data)

Upstream product

• 83-33-0 inden-1-one 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 

Downstream Products

• 1006-27-5 1-methoxyindane 
• 95-13-6 1-indene 
• 26461-03-0 1-phenylindane 
• 93010-30-1 1-(o-tolyl)-2,3-dihydro-1H-indene 
• 86043-04-1 1-(4-(trifluoromethyl)phenyl)-2,3-dihydro-1H-indene 
• 38199-89-2 1-(4-methoxyphenyl)-2,3-dihydro-1-H indene 
• 26452-97-1 1-cyanoindane 
• 87694-38-0 Indeno<1,2-d>-1,2,3-thiadiazol-8-on 
• 83-33-0 inden-1-one 

Relevant articles and documents

Indan-C60: From a crystalline molecule to photovoltaic application

Crystalline Indan-C60 and its photovoltaic application were studied. Microsheets and aloe-like micro-nano superstructures can be assembled from Indan-C60. Indan-PC61BM derived from Indan-C 60 was further investigated as an acceptor for OPV devices, which shows a higher Voc, FF, and PCE than those obtained using PC 61BM.

Synthesis of 1-aryl- benzocycloalkane derivatives via one-pot two-step reaction of benzocyclonone, tosylhydrazide, and arylboronic acid

A metal-free one-pot two-step reductive coupling reaction of benzocyclonone, tosylhydrazide, and arylboronic acid was developed for the formation of a C(sp3)–C(sp2) bond, which enabled the efficient synthesis of 1-aryl-benzocycloalkane compounds in moderate to good yields on a multi-gram scale. Moreover, five- and six-membered benzocyclic ketones are also suitable substrates for this reaction. Notably, this protocol was also found to be suitable for synthesizing 3-(3,4-dichlorophenyl)-2,3-dihydro-1H-inden-1-one, an important intermediate in the synthesis of indatraline.

Copper-Catalyzed Cyanation of N-Tosylhydrazones with Thiocyanate Salt as the "cN" Source

A novel protocol for the synthesis of α-aryl nitriles has been successfully achieved via a copper-catalyzed cyanation of N-tosylhydrazones employing thiocyanate as the source of cyanide. The features of this method include a convenient operation, readily available substrates, low-toxicity thiocyanate salts, and a broad substrate scope.