55682-13-8

Basic information

• Product Name: O-(2-iodophenyl)-N,N-dimethylcarbamate
• Synonyms: O-(2-iodophenyl)-N,N-dimethylcarbamate
• CAS NO: 55682-13-8
• Molecular Weight: 291.088
• Mol File: 55682-13-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: O-(2-iodophenyl)-N,N-dimethylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: O-(2-iodophenyl)-N,N-dimethylcarbamate(55682-13-8)
• EPA Substance Registry System: O-(2-iodophenyl)-N,N-dimethylcarbamate(55682-13-8)

Safety Data

• Hazardous Substances Data: 55682-13-8(Hazardous Substances Data)

Upstream product

• 1360939-08-7 2-deuterio-phenyl dimethylcarbamate 
• 95-56-7 2-hydroxybromobenzene 
• 533-58-4 2-Iodophenol 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 
• 23951-01-1 <2-D>-phenol 
• 108-95-2 phenol 
• 6969-90-0 phenyl N,N-dimethylcarbamate 

Downstream Products

• 945-57-3 2-cyanophenyl dimethylcarbamate 

Relevant articles and documents

Pd(II) catalyzed ortho C-H iodination of phenylcarbamates at room temperature using cyclic hypervalent iodine reagents

A novel approach to access ortho iodinated phenols using cyclic hypervalent iodine reagents through palladium(II) catalyzed C-H activation has been developed through weak coordination. The reaction showed excellent regioselectivity, reactivity and good functional group tolerance. A unique mechanism was proposed.

Suppressing the anionic fries rearrangement of aryl dialkylcarbamates; the isolation of a crystalline ortho-deprotonated carbamate

In the presence of organolithium bases phenyl dialkylcarbamates have previously been shown to undergo facile rearrangement to yield the corresponding salicylamides. However, heterometallic lithium diethyl(2,2,6,6- tetramethylpiperidido)zincate achieves th