Benzo[f]quinoline Benzo[f]quinoline

Structural formula

• Numbering system
• Physical property data
• Toxicological data
• Ecological data
• Molecular structure data
• Computing chemical data
• More
  • Properties and Stability
  • Storage method
  • Synthesis method
  • Purpose

Numbering system

CAS number:85-02-9

MDL number:MFCD00022235

EINECS number:201-582-0

RTECS number:DK1428000

BRN number:None

PubChem ID:None

Physical property data

1. Character:Nearly colorless crystal.

2. Density (g/mL,25/4 ℃):1.005(20/4℃)

3. Relative vapor density (g/mL,AIR=1): Undetermined

4. Melting point (ºC):111 ℃

5. Boiling point (ºC,Normal pressure):345-346℃

6. Boiling point (ºC,5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash Point (ºC): Undetermined

9. Specific optical rotation (º): Undetermined

10. Autoignition point or ignition temperature (ºC12, Determine the stereocenter of chemical bonds Quantity: 0

13. Uncertain number of chemical bond stereocenters:0

14. Number of covalent bond units:1

Properties and stability

Nearly colorless crystals. It is slightly alkaline. There is a spicy smell and a burning taste. Dilute solutions of acridine and its salts have green or purple fluorescence respectively. Coal tar contains acridine, mainly concentrated in an anthracene oil fraction.

Storage method

This product should be sealed and stored away from light.

Synthesis method

Prepared from acridone. Acridone is composed of diphenylamine-2- Carboxylic acid is obtained by ringing with sulfuric acid, and then reduced with pentanol and sodium to form9,10-Dioxoacridine is oxidized to obtain acridine. For laboratory preparation, acridone can also be mixed with zinc powder and heated. The acridine sublimation product generated by the reaction is dissolved in hydrochloric acid, and then alkalized with sodium hydroxide solution to precipitate and filter to obtain a crude product. Recrystallizing with methanol gives a melting point of 110 ℃‘s finest products.

Purpose

Reagents for the determination of cadmium, germanium, cobalt, bismuth and zinc.
The structure of acridine is similar to that of anthracene, and its chemical properties are also very close. After the hydrogen on the benzene ring of acridine is replaced by an amino group, it is an intermediate of acridine dye. Among acridine compounds, some have antiseptic properties and can be used as medicines, such as acriflavine and adipine.

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The structure of acridine is similar to that of anthracene, and its chemical properties are also very close. After the hydrogen on the benzene ring of acridine is replaced by an amino group, it is an intermediate of acridine dye. Among acridine compounds, some have antiseptic properties and can be used as medicines, such as acriflavine and adipine.