27017-70-5

Basic information

• Product Name: 1,5-dihydro-1,5-Naphthyridine-2,6-dione
• Synonyms: 1,5-dihydro-1,5-Naphthyridine-2,6-dione
• CAS NO: 27017-70-5
• Molecular Formula: C8H6N2O2
• Molecular Weight: 162.14544
• Mol File: 27017-70-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 360 °C (approx)
• Boiling Point: 557.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.43±0.1 g/cm3(Predicted)
• PKA: 9.97±0.20(Predicted)
• CAS DataBase Reference: 1,5-dihydro-1,5-Naphthyridine-2,6-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-dihydro-1,5-Naphthyridine-2,6-dione(27017-70-5)
• EPA Substance Registry System: 1,5-dihydro-1,5-Naphthyridine-2,6-dione(27017-70-5)

Safety Data

• Hazardous Substances Data: 27017-70-5(Hazardous Substances Data)

Usage

Type of compound

Heterocyclic compound

Usage

Pharmaceutical and organic synthesis processes

Physical appearance

Yellow powder

Solubility

Soluble in organic solvents, insoluble in water

Potential application

Antibacterial agent

Antimicrobial properties

Studied for its potential as an antimicrobial agent

Structural uniqueness

Unique structure contributes to its potential biological activity

Field of interest

Drug discovery and medicinal chemistry

Derivatives

Investigated for potential use in treating various diseases and conditions

Specific conditions

Cancer and infectious diseases
These properties and contents provide a comprehensive overview of 1,5-dihydro-1,5-naphthyridine-2,6-dione, highlighting its potential applications and areas of interest in the pharmaceutical and medicinal chemistry fields.

Upstream product

• 27017-66-9 2,6-dichloro-1,5-naphthyridine 
• 462-08-8 pyridin-3-ylamine 
• 254-79-5 1,5-naphthyridine 
• 27305-49-3 1,5-naphthyridine 1,5-dioxide 
• 6628-77-9 6-methoxy-pyridin-3-ylamine 
• 135795-46-9 2-bromo-6-methoxy-pyridin-3-ylamine 
• 27017-64-7 6-methoxy-1,5-naphthyridin-2(1H)-one 

Relevant articles and documents

A novel bis-lactam acceptor with outstanding molar extinction coefficient and structural planarity for donor-acceptor type conjugated polymer

A novel electron-accepting bis-lactam building block, 3,7-dithiophen-2-yl-1,5-dialkyl-1,5-naphthyridine-2,6-dione (NTDT), and a conjugated polymer P(NTDT-BDT) comprising NTDT as an electron acceptor and benzo[1,2-b:4,5-b′]dithiophene (BDT) as an electron donor are designed and synthesized for producing efficient organic solar cells. The thermal, electronic, photophysical, electrochemical, and structural characteristics of NTDT and P(NTDT-BDT) are studied in detail and compared with those of the widely used bis-lactam acceptor 3,6-dithiophen-2-yl-2,5-dialkylpyrrolo[3,4-c]pyrrole-1,4-dione (DPPT) and its polymer P(DPPT-BDT). Compared to DPPT derivatives, NTDT and P(NTDT-BDT) exhibit remarkably higher absorption coefficients, deeper highest occupied molecular orbital energy levels, and more planar conformations. A bulk heterojunction solar cells based on P(NTDT-BDT) exhibit power conversion efficiency of up to 8.16% with high short circuit current (Jsc) of 18.51 mA cm-2, one of the highest Jsc values yet obtained for BDT-based polymer. Thus, it is successfully demonstrated that the novel bis-lactam unit NTDT is a promising building block for use in organic photovoltaic devices.