480450-72-4

Basic information

• Product Name: methyl 2-[(4-bromophenyl)amino]-2-oxoacetate
• Synonyms: methyl 2-[(4-bromophenyl)amino]-2-oxoacetate
• CAS NO: 480450-72-4
• Molecular Formula: C₉H₈BrNO₃
• Molecular Weight: 258.06872
• Mol File: 480450-72-4.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 2-[(4-bromophenyl)amino]-2-oxoacetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-[(4-bromophenyl)amino]-2-oxoacetate(480450-72-4)
• EPA Substance Registry System: methyl 2-[(4-bromophenyl)amino]-2-oxoacetate(480450-72-4)

Safety Data

• Hazardous Substances Data: 480450-72-4(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 5781-53-3 monomethyl oxalyl chloride 
• 106-40-1 4-bromo-aniline 
• 107504-22-3 dimethyl 2-((4-bromophenyl)amino)but-2-enedioate 

Downstream Products

• 1307704-30-8 1-(4-bromophenyl)indoline-2,3-dione 
• 79354-51-1 4-bromooxanilic acid 

Relevant articles and documents

Metal-Free Oxidative C=C Bond Cleavage of Electron-Deficient Enamines Promoted by tert -Butyl Hydroperoxide

A novel tert -butyl hydroperoxide (TBHP)-promoted oxidative C=C double-bond cleavage of enamines is described. Heating a solution of an electron-deficient enamine in chlorobenzene at 80 °C in the presence of TBHP for two hours led to cleavage of the C=C bond. This study offers a new strategy to carry out C=O double-bond formation by the use of TBHP.

PAI-1 INHIBITOR

The compound represented by the following formula (I) and the like have PAI-1 inhibition activity; wherein: R1 represents a C6-10 aryl group which may be substituted or the like; T represents a single bond or the like; m represents 0

Synthesis of methyl N-aryl oxamate using soluble polymer support

A variety of methyl N-aryl oxamates were synthesized using poly(ethylene glycol) (PEG) as a soluble polymer support and a monoproctection group with excellent yields. Copyright Taylor & Francis Group, LLC.