AI52870
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
5g | 98% | in stock | $8.00 | $6.00 | - + | |
10g | 98% | in stock | $10.00 | $7.00 | - + | |
25g | 98% | in stock | $18.00 | $13.00 | - + | |
100g | 98% | in stock | $44.00 | $31.00 | - + | |
500g | 98% | in stock | $217.00 | $152.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AI52870 |
Chemical Name: | N-(2-Bromoethyl)phthalimide |
CAS Number: | 574-98-1 |
Molecular Formula: | C10H8BrNO2 |
Molecular Weight: | 254.0800 |
MDL Number: | MFCD00005902 |
SMILES: | BrCCN1C(=O)c2c(C1=O)cccc2 |
NSC Number: | 2688 |
Complexity: | 243 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 2 |
XLogP3: | 2.2 |
The compound 2-(2-Bromoethyl)isoindoline-1,3-dione serves as a valuable building block in chemical synthesis due to its versatile reactivity and functional groups. This compound can be utilized as a key intermediate for the synthesis of various chemical compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its halogenated moiety enables it to participate in nucleophilic substitution reactions, allowing for the introduction of different functional groups. Additionally, the isoindoline-1,3-dione core structure offers a unique scaffold for further elaboration through a variety of synthetic transformations, such as cyclization, cross-coupling, and ring-opening reactions. This compound's broad synthetic utility makes it a valuable tool in the development of novel molecules with potential applications in drug discovery, materials science, and other fields of chemical research.
Acta crystallographica. Section E, Structure reports online 20111101
Bioorganic & medicinal chemistry 20091001