CAS 140715-56-6
:2-(3-bromopropyl)-5-nitroisoindoline-1,3-dione
Description:
2-(3-Bromopropyl)-5-nitroisoindoline-1,3-dione, identified by its CAS number 140715-56-6, is a synthetic organic compound characterized by its isoindoline structure, which features a nitro group and a bromopropyl substituent. This compound typically exhibits a yellow to orange color due to the presence of the nitro group, which can influence its electronic properties and reactivity. The bromopropyl group introduces a halogen, enhancing its potential for further chemical modifications and applications in organic synthesis. The presence of the dione functional groups suggests that it may participate in various chemical reactions, such as nucleophilic additions or cycloadditions. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Its solubility and stability can vary depending on the solvent and environmental conditions, which are important factors for its practical applications. Overall, this compound represents a versatile building block in organic synthesis and may have potential applications in pharmaceuticals or agrochemicals.
Formula:C11H9BrN2O4
InChI:InChI=1/C11H9BrN2O4/c12-4-1-5-13-10(15)8-3-2-7(14(17)18)6-9(8)11(13)16/h2-3,6H,1,4-5H2
SMILES:C(CBr)CN1C(=O)c2ccc(cc2C1=O)N(=O)=O
Synonyms:- 2-(3-bromopropyl)-5-nitro-1H-isoindole-1,3(2H)-dione
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
1H-Isoindole-1,3(2H)-dione, 2-(3-bromopropyl)-5-nitro-
CAS:Formula:C11H9BrN2O4Molecular weight:313.1042N-(3-Bromoprop-1-yl)-4-nitrophthalimide
CAS:<p>N-(3-Bromoprop-1-yl)-4-nitrophthalimide</p>Purity:97%Molecular weight:313.10g/mol

