909397-79-1

Basic information

• Product Name: 1H-Pyrrole-2,5-dione, 3-bromo-1-[(3,4-dimethoxyphenyl)methyl]-
• CAS NO: 909397-79-1
• Molecular Formula: C13H12BrNO4
• Molecular Weight: 326.147
• Mol File: 909397-79-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-2,5-dione, 3-bromo-1-[(3,4-dimethoxyphenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2,5-dione, 3-bromo-1-[(3,4-dimethoxyphenyl)methyl]-(909397-79-1)
• EPA Substance Registry System: 1H-Pyrrole-2,5-dione, 3-bromo-1-[(3,4-dimethoxyphenyl)methyl]-(909397-79-1)

Safety Data

• Hazardous Substances Data: 909397-79-1(Hazardous Substances Data)

Upstream product

• 5926-51-2 bromomaleic anhydride 
• 5763-61-1 3,4-dimethoxybenzylamine 

Downstream Products

• 923982-30-3 C₁₉H₁₅F₂NO₄ 
• 923982-42-7 C₂₀H₁₈FNO₄ 
• 923982-39-2 C₂₀H₁₈FNO₄ 
• 923982-45-0 C₂₃H₁₉NO₄ 
• 1474012-78-6 C₂₇H₂₁FN₂O₄ 
• 1474012-74-2 C₂₂H₁₆F₄N₂O₄ 
• 1474012-69-5 C₂₂H₁₆ClF₃N₂O₄ 
• 1474012-65-1 C₂₂H₁₇F₃N₂O₄ 
• 923982-36-9 C₂₀H₁₈FNO₅ 
• 923982-51-8 C₂₅H₂₃NO₅ 
• 923982-48-3 C₂₄H₂₁NO₅ 
• 923982-54-1 C₂₄H₂₁NO₄ 

Relevant articles and documents

A tandem [3+2] cycloaddition-elimination cascade reaction to generate pyrrolo-[3,4-c]pyrrole-1,3-diones

An efficient tandem [3+2] cycloaddition-elimination cascade sequence has been developed enabling assembly of the pharmacologically relevant pyrrolo-[3,4-c]pyrrole-1,3-dione chemotype. The strategy involves simple mixing of readily accessible oxazolin-2-on

METHODS AND COMPOSITIONS FOR PRODUCTION, FORMULATION AND USE OF 1-ARYL-3-AZABICYCLO[3.1.0] HEXANES

The invention provides novel l-aryl-3-azabicyclo[3.1.0] hexanes that are active for modulating biogenic amine transport, along with compositions and methods for using these compounds to treat central nervous system disorders. Certain l-aryl-3-azabicyclo[3.1.0] hexanes are provided that have at least one substituent on the aryl ring. In other embodiments l-aryl-3-azabicyclo[3.1.0] hexanes are provided that have a substitution on the nitrogen at the '3' position. In additional embodiments l-aryl-3-azabicyclo[3.1.0] hexanes are provided which have one substitution on the aryl ring, as well as a substitution on the nitrogen at the '3' position. The invention also provides novel methods of making aryl- and aza-substituted l-aryl-3-azabicyclo[3.1.0] hexanes, including synthetic methods that form novel intermediate compounds of the invention for producing aryl- and aza-substituted l-aryl-3-azabicyclo[3.1.0] hexanes.