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2,3-dihydrofluoranthene
- Name: 2,3-dihydrofluoranthene
- CAS: 30339-87-8
- Purity: 99%
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Description
2,3-dihydrofluoranthene Good Supplier In Bulk Supply High Purity 30339-87-8
- Molecular Formula: C16H12
- Molecular Weight: 204.271
- Vapor Pressure: 2.73E-05mmHg at 25°C
- Boiling Point: 368.3°Cat760mmHg
- Flash Point: 190.9°C
- PSA： 0.00000
- Density: 1.19g/cm3
- LogP: 4.04490
2,3-dihydrofluoranthene(Cas 30339-87-8) Usage
Type of compound
2,3-dihydrofluoranthene is a polycyclic aromatic hydrocarbon (PAH) compound.
Physical appearance
It is a white to light yellow solid.
Melting point
2,3-dihydrofluoranthene has a melting point of 127-129°C.
Usage
It is primarily used as a precursor in the synthesis of various organic compounds and materials.
Mutagenic properties
2,3-dihydrofluoranthene is known to be mutagenic, meaning it can cause changes in the genetic material of living organisms.
Carcinogenic properties
2,3-dihydrofluoranthene is also carcinogenic, which means it has the potential to cause cancer in living organisms.
Toxic effects
Exposure to 2,3-dihydrofluoranthene can exhibit toxic effects on living organisms.
Regulation and monitoring
Due to its potential health hazards, 2,3-dihydrofluoranthene is regulated and monitored in industrial applications to minimize exposure and environmental impact.
General Description
2,3-dihydrofluoranthene is a polycyclic aromatic hydrocarbon (PAH) compound with a chemical formula C16H12. It is a white to light yellow solid with a melting point of 127-129°C. 2,3-dihydrofluoranthene is primarily used as a precursor in the synthesis of various organic compounds and materials. It is also known to be a mutagenic and carcinogenic compound, exhibiting toxic effects on living organisms. Due to its potential health hazards, 2,3-dihydrofluoranthene is regulated and monitored in industrial applications to minimize exposure and environmental impact.
InChI:InChI=1/C16H12/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-3,5,7-10H,4,6H2
30339-87-8 Relevant articles
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Streitwieser,A.,Suzuki,S.
, p. 153 - 168 (1961)
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Harvey,R.G. et al.
, p. 2909 - 2919 (1972)
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Synthesis and characterization of nitro-, nitroso-, and aminofluoranthenes
Haeringen, C. J. van,Aten, N. F.,Cornelisse, J.,Lugtenburg, J.
, p. 335 - 344 (2007/10/02)
The synthesis is reported of the five mo...
Fluoranthene: Synthesis and Mutagenicity of Four Diol Epoxides
Rastetter, William H.,Nachbar, Robert B.,Russo-Rodriguez, Sandra,Wattley, Ruth V.,Thilly, William G.,et al.
, p. 4873 - 4878 (2007/10/02)
The syntheses of diol epoxides 4a,b and ...
30339-87-8 Process route
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206-44-0
fluoranthene
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30339-87-8
2,3-Dihydrofluoranthene
ConditionsConditions Yield With ammonia; sodium; In tetrahydrofuran; at -50 ℃; for 0.416667h;100%
Multistep reaction; (i) Li, liq. NH3, (ii) NaOMe, MeOH;-
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20279-21-4
1,2,3,10b-tetrahydrofluoranthene
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30339-87-8
2,3-Dihydrofluoranthene
ConditionsConditions Yield Multistep reaction; (i) nBuLi, benzene, heptane, (ii) O2, (iii) HCl, AcOH;Multi-step reaction with 2 steps1: O2 , KOH, 18-crown-6 / benzene / 24 h2: CH3 SO3 H / CH2 Cl2With potassium hydroxide; methanesulfonic acid; 18-crown-6 ether; oxygen; In dichloromethane; benzene;30339-87-8 Upstream products
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206-44-0
fluoranthene
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20279-21-4
1,2,3,10b-tetrahydrofluoranthene
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31398-92-2
5,6-dihydrofluoranthen-6a(4H)-ol
30339-87-8 Downstream products
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33543-31-6
2-methylfluoranthene
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33611-88-0
1,2-dinitrofluoranthene
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85923-83-7
1,10b-epoxy-1,2,3,10b-tetrahydrofluoranthene
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83291-45-6
(1R,10bS)-2,3-Dihydro-1H-fluoranthene-1,10b-diol
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