155060-13-2

Basic information

• Product Name: 4-Nitro-benzenesulfonic acid 1-oxo-indan-2-yl ester
• CAS NO: 155060-13-2
• Molecular Weight: 333.321
• Mol File: 155060-13-2.mol

Chemical Properties

• CAS DataBase Reference: 4-Nitro-benzenesulfonic acid 1-oxo-indan-2-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Nitro-benzenesulfonic acid 1-oxo-indan-2-yl ester(155060-13-2)
• EPA Substance Registry System: 4-Nitro-benzenesulfonic acid 1-oxo-indan-2-yl ester(155060-13-2)

Safety Data

• Hazardous Substances Data: 155060-13-2(Hazardous Substances Data)

Upstream product

• 138-42-1 p-nitrobenzenesulfonic acid 
• 83-33-0 inden-1-one 
• 61477-33-6 [hydroxy(p-nitrobenezenesulfonyloxy)iodo]benzene 
• 19455-83-5 1H-inden-3-yl acetate 
• 6209-72-9 4-nitrobenzenesulfonyl peroxide 

Downstream Products

• 113021-30-0 2-iodo-1-indanone 
• 1579-20-0 2-ethoxy-1-indanone 

Relevant articles and documents

Highly Efficient α-Organosulfonyloxylation of Carbonyl Compounds under Microwave Irradiation

Iodobenzene diacetate and organosulfonic acid mediated reaction of various carbonyl compounds under solventless microwave irradiation provided α-organosulfonyloxy carbonyl compounds in high yields.

An effective synthesis of α-azido ketones from ketones

One-pot transformation of ketones into α-azido ketones has been achieved by successive treatment with HNIB and NaN3 in acetonitrile.

Efficient method for α-iodination of ketones

α-Iodoketones are prepared in high yields from the initial reaction of various ketones with HNIB in CH3CN and subsequent treatment of potassium iodide or samarium(II) iodide.

A facile synthesis of secondary α-alkoxy or α-acetoxy aromatic ketones

The treatment of HNIB with aromatic ketones and subsequent solvolysis using alcohol or acetic acid in one-pot system makes it possible to give corresponding secondary α-alkoxy or α-acetoxy ketones in high yields.