CAS 65060-93-7
:1H-Pyrrole-2,5-dione, 3-bromo-1-methyl-
Description:
1H-Pyrrole-2,5-dione, 3-bromo-1-methyl- is a chemical compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. The presence of the bromine atom at the 3-position and a methyl group at the 1-position contributes to its unique reactivity and properties. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry and organic synthesis. It is likely to be a solid at room temperature and may have moderate solubility in organic solvents. The presence of the dione functional groups suggests it can participate in various chemical reactions, including nucleophilic additions and cycloadditions. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the bromine and methyl substituents. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 1H-Pyrrole-2,5-dione, 3-bromo-1-methyl- is a versatile compound with potential applications in various fields of chemistry.
Formula:C5H4BrNO2
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Found 3 products.
3-Bromo-1-methyl-2,5-dihydro-1h-pyrrole-2,5-dione
CAS:Formula:C5H4BrNO2Purity:97%Molecular weight:189.99483-Bromo-1-methyl-1H-pyrrole-2,5-dione
CAS:<p>3-Bromo-1-methyl-1H-pyrrole-2,5-dione</p>Purity:97%Molecular weight:190g/mol3-Bromo-1-methyl-2,5-dihydro-1H-pyrrole-2,5-dione
CAS:<p>3-Bromo-1-methyl-2,5-dihydro-1H-pyrrole-2,5-dione is a fluorescent molecule that can be used as a phosphine. It has been shown to be a useful tool for investigating the nature of phosphines and their reactions with other molecules. This compound has also been used in the kinetic modification of drugs to optimise their therapeutic properties. 3-Bromo-1-methyl-2,5-dihydro-1H-pyrrole-2,5-dione has been conjugated with biotin to create a reactive disulfide bond that can be visualised using fluorescent microscopy. The unmodified form of 3BMPD is used in molecular modelling studies as a model system for reactive disulfide bonds. 3BMPD can also be modified by reacting it with thiols or maleimides to produce reactive disulfides that are useful in conjug</p>Formula:C5H4BrNO2Purity:Min. 95%Molecular weight:189.99 g/mol



