5198-51-6

Basic information

• Product Name: N-(3-nitrophenyl)oxazolidin-2-one
• Synonyms: N-(3-nitrophenyl)oxazolidin-2-one
• CAS NO: 5198-51-6
• Molecular Weight: 208.174
• Mol File: 5198-51-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-(3-nitrophenyl)oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-nitrophenyl)oxazolidin-2-one(5198-51-6)
• EPA Substance Registry System: N-(3-nitrophenyl)oxazolidin-2-one(5198-51-6)

Safety Data

• Hazardous Substances Data: 5198-51-6(Hazardous Substances Data)

Upstream product

• 96-49-1 [1,3]-dioxolan-2-one 
• 99-09-2 3-nitro-aniline 
• 124-38-9 carbon dioxide 
• 107-06-2 1,2-dichloro-ethane 
• 497-25-6 dimethylenecyclourethane 
• 645-00-1 m-iodonitrobenzene 
• 60480-06-0 1-chloro-2-(4-nitro-phenylcarbamoyloxy)-ethane 

Downstream Products

• 31847-21-9 3-(3-{4-[bis-(2-chloro-ethyl)-amino]-2-methyl-benzylideneamino}-phenyl)-oxazolidin-2-one 
• 31847-20-8 3-(3-{4-[bis-(2-chloro-ethyl)-amino]-benzylideneamino}-phenyl)-oxazolidin-2-one 
• 31847-14-0 3-(4-{4-[bis-(2-chloro-ethyl)-amino]-2-methyl-benzylideneamino}-phenyl)-oxazolidin-2-one 
• 31847-12-8 3-(4-{4-[bis-(2-chloro-ethyl)-amino]-benzylideneamino}-phenyl)-oxazolidin-2-one 
• 34232-43-4 3-(3-aminophenyl)oxazolidin-2-one 

Relevant articles and documents

MODIFIED PROTEINS AND PROTEIN DEGRADERS

Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.

Synthesis of Oxazolidinones and Derivatives through Three-Component Fixation of Carbon Dioxide

An effective three-component fixation of atmospheric CO2 with readily available 1,2-dichloroethane and aromatic amine toward oxazolidinones catalyzed by in situ NHC was developed. The reaction occurred in good to excellent yields with good gene

An eco-friendly, convenient, and practical conversion of arylamines to oxazolidinones

A one-step procedure for efficient synthesis of oxazolidinone only using ethylene carbonate and arylamines in the presence of 1,4-diazabicyclo[2,2,2] octane (DABCO) was developed. In most cases, moderate to high yield of products were obtained. This reaction can be considered a carbon dioxide fixation reaction since ethylene carbonate was synthesized via reaction of ethylene oxide with carbon dioxide. Copyright