2955-74-0

Basic information

• Product Name: ethyl {[(4-nitrophenyl)sulfonyl]oxy}carbamate
• CAS NO: 2955-74-0
• Molecular Formula: C₉H₁₀N₂O₇S
• Molecular Weight: 290.2499
• Mol File: 2955-74-0.mol
• Article Data: 1

Chemical Properties

• Density: 1.49g/cm³
• Refractive Index: 1.557
• CAS DataBase Reference: ethyl {[(4-nitrophenyl)sulfonyl]oxy}carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl {[(4-nitrophenyl)sulfonyl]oxy}carbamate(2955-74-0)
• EPA Substance Registry System: ethyl {[(4-nitrophenyl)sulfonyl]oxy}carbamate(2955-74-0)

Safety Data

• Hazardous Substances Data: 2955-74-0(Hazardous Substances Data)

Upstream product

• 589-41-3 ethyl N-hydroxylcarbamate 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 

Downstream Products

• 13640-77-2 2-ethoxycarbonylaminocyclohexanone 
• 98945-58-5 Morpholin-4-yl-carbamic acid ethyl ester 
• 98945-55-2 C₁₃H₂₂N₂O₃ 
• 83487-79-0 1-<(ethoxycarbonyl)amino>pyrrolidine 
• 83487-80-3 C₁₃H₂₂N₂O₂ 
• 233256-39-8 2-(ethoxycarbonyl)-2-(ethoxycarbonylamino)cyclohexanone 
• 881691-01-6 (2-methylene-3-oxobutyl)carbamic acid ethyl ester 

Relevant articles and documents

Pd-catalyzed intermolecular ortho-C-H amidation of anilides by N-nosyloxycarbamate

A palladium-catalyzed ortho-C-H amidation of anilides by N-nosyloxycarbamates was developed for the synthesis of 2-aminoanilines. This reaction can be carried out under relatively mild conditions and exhibits excellent regioselectivity and functional group tolerance. The amidation reaction is probably initiated by rate-limiting C-H cyclopalladation (k H/kD = 3.7) to form an arylpalladium complex, followed by nitrene functionalization.