Chemical Name: | 1H-Isoindole-1,3(2H)-dione, 5-bromo-6-nitro- |
CAS Number: | 64823-14-9 |
Product Number: | AG00F797(AGN-PC-0L0RLC) |
Synonyms: | |
MDL No: | |
Molecular Formula: | C8H3BrN2O4 |
Molecular Weight: | 271.02442 |
5-Bromo-6-nitroisoindoline-1,3-dione is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound plays a crucial role in the development and design of various organic molecules, particularly in the pharmaceutical and agrochemical industries. In chemical synthesis, 5-Bromo-6-nitroisoindoline-1,3-dione serves as a key building block for the construction of complex organic structures due to its ability to undergo a variety of reactions. It participates in nucleophilic substitution reactions, where the bromo and nitro groups can be selectively modified to introduce new functional groups at specific positions on the molecule. This flexibility allows for the fine-tuning of desired chemical properties in the final product. Furthermore, the presence of both a bromo and nitro group in 5-Bromo-6-nitroisoindoline-1,3-dione enables it to act as a versatile synthetic intermediate in the creation of heterocyclic compounds. By manipulating the structure of this compound through various synthetic strategies, chemists can access a diverse range of target molecules with specific pharmacological or biological activities. Overall, the strategic incorporation of 5-Bromo-6-nitroisoindoline-1,3-dione in chemical synthesis offers researchers a powerful tool for the efficient and precise construction of complex organic compounds with tailored properties and functionalities.