38528-41-5

Basic information

• Product Name: 2-{[3-(dibutylamino)propyl]amino}naphthalene-1,4-dione
• Synonyms: 2-([3-(Dibutylamino)propyl]amino)naphthoquinone; 2-[3-[Di-n-butylamino]propylamino]-1,4-naphthoquinone
• CAS NO: 38528-41-5
• Molecular Formula: C₂₁H₃₀N₂O₂
• Molecular Weight: 342.4751
• Mol File: 38528-41-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 479.1°C at 760 mmHg
• Flash Point: 243.6°C
• Density: 1.07g/cm³
• Vapor Pressure: 2.43E-09mmHg at 25°C
• Refractive Index: 1.553
• CAS DataBase Reference: 2-{[3-(dibutylamino)propyl]amino}naphthalene-1,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{[3-(dibutylamino)propyl]amino}naphthalene-1,4-dione(38528-41-5)
• EPA Substance Registry System: 2-{[3-(dibutylamino)propyl]amino}naphthalene-1,4-dione(38528-41-5)

Safety Data

• Hazardous Substances Data: 38528-41-5(Hazardous Substances Data)

Usage

Properties

1. Molecular formula: C22H28N2O2
2. Contains a dibutylamino group and a propylamino group attached to the naphthalene ring
3. Likely a fluorescent dye or probe
4. Potential applications in biochemical and medical research
5. May be used for staining and imaging biological samples
6. Studying cellular processes

Specific Content

Contains dibutylamino and propylamino groups
Likely a fluorescent dye or probe
Applications in biochemical and medical research
Potential uses in staining and imaging biological samples
Studying cellular processes
Further research needed to understand properties and uses

Upstream product

• 102-83-0 3-dibutylaminopropylamine 
• 130-15-4 [1,4]naphthoquinone 
• 571-60-8 1,4-Dihydroxynaphthalene 

Relevant articles and documents

Anticancer Activity of 2-Amino-substituted-1,4-naphthoquinone Derivatives in Ovarian Cancer Cells

2-Amino-substituted-1,4-naphthoquinone derivatives (10–17) were synthesized from coupling reaction between 1,4-dihydroxynaphthalene and amines in the presence of catalyst CeCl3.7H2O. Their anticancer activity was evaluated by using three ovarian cancer cells (A2780, SKOV3, and OVCAR3). Among the eight compounds, compound 13 containing metal chelating moiety had a relatively potent cytotoxic activity (IC50 10 μM) on all three ovarian cancer cells.

Synthesis and screening of substituted 1,4-naphthoquinones (NPQs) as antifilarial agents

Eleven amino-substituted 1,4-naphthoquinones were synthesized via the reaction of 1,4-naphthoquinone with different primary and secondary mono- and diamines in the presence of dichloromethane ethanol (1:2) solvent at room temperature. All compounds were p