1-Fluoronaphthalene structure
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Common Name | 1-Fluoronaphthalene | ||
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CAS Number | 321-38-0 | Molecular Weight | 146.161 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 215.0±0.0 °C at 760 mmHg | |
Molecular Formula | C10H7F | Melting Point | −13 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 65.6±0.0 °C | |
Symbol |
GHS08 |
Signal Word | Warning |
Use of 1-Fluoronaphthalene1-Fluoronaphthalene is an organofluorine compound derived from naphthalene derivatives and fluorinated aromatics. 1-Fluoronaphthalene can be used to synthesize LY248686, a potent inhibitor of serotonin and noradrenaline uptake[1]. |
Name | Fluoronaphthalene |
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Synonym | More Synonyms |
Description | 1-Fluoronaphthalene is an organofluorine compound derived from naphthalene derivatives and fluorinated aromatics. 1-Fluoronaphthalene can be used to synthesize LY248686, a potent inhibitor of serotonin and noradrenaline uptake[1]. |
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Related Catalog | |
In Vitro | 1-Fluoronaphthalene (3 mg, 24 h) can be oxidized by C.elegans ATCC 36112 to form trans-3,4-dihydroxy-3,4-dihydro-1-fluoronaphthalene and trans-5,6-dihydroxy-5,6-dihydro-1-fluoronaphthalene and to form 1-fluoro-8-hydroxy-5-tetralone, 5-hydroxy-1-fluoronaphthalene and 4-hydroxy-1-fluoronaphthalene as well as glucosides, sulfates and glucuronide conjugates of these phenols[1]. |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 215.0±0.0 °C at 760 mmHg |
Melting Point | −13 °C(lit.) |
Molecular Formula | C10H7F |
Molecular Weight | 146.161 |
Flash Point | 65.6±0.0 °C |
Exact Mass | 146.053177 |
LogP | 3.50 |
Vapour Pressure | 0.2±0.4 mmHg at 25°C |
Index of Refraction | 1.606 |
Stability | Stable. Incompatible with strong oxidizing agents. |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS08 |
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Signal Word | Warning |
Hazard Statements | H351 |
Precautionary Statements | P281 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36-S36/37-S24/25-S23-S53 |
RIDADR | UN 2810 |
WGK Germany | 3 |
RTECS | QJ7100000 |
HS Code | 2903999090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2903999090 |
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Summary | 2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Synthesis of highly oxygenated dinaphthyl ethers via SNAr reactions promoted by Barton's base.
Org. Lett. 5(7) , 1155-8, (2003) [reaction: see text] Electron-rich dinaphthyl ethers were synthesized by S(N)Ar reactions between naphthols and activated fluoronaphthalenes. 2-tert-Butyl-1,1,3,3-tetramethylguanidine (Barton's base) ... |
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Effects of a fluoro substituent on the fungal metabolism of 1-fluoronaphthalene.
Appl. Environ. Microbiol. 48(2) , 294-300, (1984) The metabolism of 1-fluoronaphthalene by Cunninghamella elegans ATCC 36112 was studied. The metabolites were isolated by reverse-phase high-pressure liquid chromatography and characterized by the appl... |
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A one-pot access to 6-substituted phenanthridines from fluoroarenes and nitriles via 1,2-arynes.
Org. Lett. 4(16) , 2687-90, (2002) [reaction: see text] A one-pot, t-BuLi-induced synthesis of 6-substituted phenanthridines from fluoroarenes and nitriles via 1,2-arynes is reported. Aryl- and hetaryl nitriles, cyanamides, and trimeth... |
1-FLUORONAPTHALENE |
α-Fluoronaphthalene |
1-fluoromaphthalene |
1-fluoro-naphthalen |
Naphthalene, 1-fluoro- |
EINECS 206-287-0 |
1-Fluornaphthalen |
4-fluoro-l-naphthalene |
I-Fluoronaphthalene |
1-Flouronaphthalene |
I-Fluornaphthalin |
L66J BF |
MFCD00003873 |
1-Fluoronaphthalene |
1-Fluornaftalen |
1-FLUORO NAPHTHALENE |