114149-17-6

Basic information

• Product Name: Benzenesulfonamide, N-(2,3-dihydro-1H-inden-2-yl)-4-methyl-
• CAS NO: 114149-17-6
• Molecular Formula: C16H17NO2S
• Molecular Weight: 287.382
• Mol File: 114149-17-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-(2,3-dihydro-1H-inden-2-yl)-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-(2,3-dihydro-1H-inden-2-yl)-4-methyl-(114149-17-6)
• EPA Substance Registry System: Benzenesulfonamide, N-(2,3-dihydro-1H-inden-2-yl)-4-methyl-(114149-17-6)

Safety Data

• Hazardous Substances Data: 114149-17-6(Hazardous Substances Data)

Upstream product

• 2338-18-3 2-aminoindane hydrochloride 
• 98-59-9 p-toluenesulfonyl chloride 
• 2975-41-9 2,3-dihydro-1H-inden-2-amine 
• 180260-72-4 2-azido-2,3-dihydro-1H-indene 
• 777-72-0 methansulfonic acid 2,3-dihydro-1H-inden-2-yl ester 
• 4254-29-9 indan-2-ol 
• 615-13-4 2-indanone 

Relevant articles and documents

Multiple Halogenation of Aliphatic C?H Bonds within the Hofmann–L?ffler Manifold

An innovative approach to position-selective polyhalogenation of aliphatic hydrocarbon bonds is presented. The reaction proceeded within the Hofmann-L?ffler manifold with amidyl radicals as the sole mediators to induce selective 1,5- and 1,6-hydrogen-atom transfer followed by halogenation. Multiple halogenation events of up to four innate C?H bond functionalizations were accomplished. The broad applicability of this new entry into polyhalogenation and the resulting synthetic possibilities were demonstrated for a total of 27 different examples including mixed halogenations.

Benzenesulphonamidoindanyl compounds, medicaments thereof, and processes of preparation

The invention relates to new benzenesulphonamidoindanyl compounds having the following formula STR1 wherein the substituents are defined herein useful in the treatment and prophylaxis of thromboembolic diseases, arteriosclerosis and tumor metastasis.