CAS 100874-09-7

4-Bromo-N-ethyl-1,8-naphthalimide

Description:

4-Bromo-N-ethyl-1,8-naphthalimide is an organic compound characterized by its naphthalimide structure, which features a naphthalene ring fused to a phthalimide moiety. The presence of a bromine atom at the 4-position of the naphthalimide enhances its reactivity and can influence its electronic properties, making it useful in various applications, including fluorescence and as a potential dye. The N-ethyl substituent contributes to the compound's solubility and may affect its biological activity. This compound is typically used in research settings, particularly in studies involving photophysical properties and as a fluorescent probe. Its molecular structure allows for interactions with biological systems, making it of interest in medicinal chemistry. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and solvent polarity. Overall, 4-Bromo-N-ethyl-1,8-naphthalimide is a versatile compound with significant implications in both synthetic and applied chemistry.

Formula: C₁₄H₁₀BrNO₂

InChI: InChI=1S/C14H10BrNO2/c1-2-16-13(17)9-5-3-4-8-11(15)7-6-10(12(8)9)14(16)18/h3-7H,2H2,1H3

InChI key: InChIKey=WNFHOJUNEAHMPD-UHFFFAOYSA-N

SMILES: O=C1C=2C=3C(C(=O)N1CC)=CC=CC3C(Br)=CC2

Synonyms:

• 1H-benz[de]isoquinoline-1,3(2H)-dione, 6-bromo-2-ethyl-
• 4-Bromo-N-ethyl-1,8-naphthalimide
• 6-Bromo-2-ethyl-1H-benz[de]isoquinoline-1,3(2H)-dione
• N-Ethyl-4-bromo-1,8-naphthalimide
• Naphthalimide, 4-bromo-N-ethyl-
• 6-Bromo-2-ethyl-1H-benzo[de]isoquinoline-1,3(2H)-dione

6-bromo-2-ethyl-1H-benzo[de]isoquinoline-1,3(2H)-dione

CAS: 100874-09-7

Formula: C₁₄H₁₀BrNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 304.1387

Ref: IN-DA0096UG

6-BROMO-2-ETHYL-1H-BENZO[DE]ISOQUINOLINE-1,3(2H)-DIONE

CAS: 100874-09-7

Purity: 95.0%

Molecular weight: 304.14300537109375

Ref: 10-F506072