Product Name

  • Name

    2-Fluoro-6-nitroanisole

  • EINECS
  • CAS No. 484-94-6
  • Article Data12
  • CAS DataBase
  • Density 1.321 g/cm3
  • Solubility
  • Melting Point 9 °C
  • Formula C7H6FNO3
  • Boiling Point 266.4 °C at 760 mmHg
  • Molecular Weight 171.128
  • Flash Point 114.9 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 484-94-6 (2-Fluoro-6-nitroanisole)
  • Hazard Symbols
  • Synonyms Anisole,2-fluoro-6-nitro- (6CI,8CI);1-Fluoro-2-methoxy-3-nitrobenzene;2-Fluoro-6-nitroanisole;1-fluoro-2-methoxy-3-nitrobenzene;2-Fluoro-6-nitro anisole;2-Fluoro-6-nitrophenyl methyl ether;benzene, 1-fluoro-2-methoxy-3-nitro-;
  • PSA 55.05000
  • LogP 2.26570

Synthetic route

1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

3-fluoro-2-methoxyaniline
437-83-2

3-fluoro-2-methoxyaniline

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In ethyl acetate for 24h;94%
With platinum Hydrogenation;
With hydrogen; palladium on activated charcoal In methanol at 20℃; for 27h;
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

2-(Diethylamino)ethanol
100-37-8

2-(Diethylamino)ethanol

N,N-diethyl-2-(2-methoxy-3-nitrophenoxy)ethanamine

N,N-diethyl-2-(2-methoxy-3-nitrophenoxy)ethanamine

Conditions
ConditionsYield
Stage #1: 2-(Diethylamino)ethanol With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.666667h;
Stage #2: 1-fluoro-2-methoxy-3-nitrobenzene In N,N-dimethyl-formamide at 20℃;		19%
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

1-bromo-2-methoxy-3-fluorobenzene
845829-94-9

1-bromo-2-methoxy-3-fluorobenzene

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
View Scheme
Multi-step reaction with 2 steps
1.1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 2844.39 Torr
2.1: sodium nitrite / water / 1 h / -5 - 0 °C
2.2: 2 h / 0 - 50 °C
View Scheme
Multi-step reaction with 2 steps
1.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / 2844.39 Torr
2.1: sodium nitrite; hydrogen bromide / water / 1 h / -5 - 0 °C
2.2: 2 h / 0 - 50 °C
View Scheme
Multi-step reaction with 2 steps
1.1: palladium 10% on activated carbon; hydrogen / methanol / 20 °C / 2844.39 Torr
2.1: hydrogen bromide; sodium nitrite / water / 1 h / -5 - 0 °C
2.2: 2 h / 0 - 50 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

4-bromo-2-fluoro-3-methoxybenzoic acid
194804-92-7

4-bromo-2-fluoro-3-methoxybenzoic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
View Scheme
Multi-step reaction with 3 steps
1.1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 2844.39 Torr
2.1: sodium nitrite / water / 1 h / -5 - 0 °C
2.2: 2 h / 0 - 50 °C
3.1: diisopropylamine; n-butyllithium / tetrahydrofuran / 1 h / -70 °C
View Scheme
Multi-step reaction with 3 steps
1.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / 2844.39 Torr
2.1: sodium nitrite; hydrogen bromide / water / 1 h / -5 - 0 °C
2.2: 2 h / 0 - 50 °C
3.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -70 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

4-bromo-2-fluoro-3-methoxybenzoic acid chloride

4-bromo-2-fluoro-3-methoxybenzoic acid chloride

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 20 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

ethyl 3-(4-bromo-2-fluoro-3-methoxyphenyl)-3-oxopropionate
194804-99-4

ethyl 3-(4-bromo-2-fluoro-3-methoxyphenyl)-3-oxopropionate

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 20 °C
5.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
5.2: 4.70 g / hexane; tetrahydrofuran; CH2Cl2 / -78 - 10 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

7-bromo-9-cyclopropyl-8-methoxy-9H-isothiazolo[5,4-b]quinoline-3,4-dione
846564-00-9

7-bromo-9-cyclopropyl-8-methoxy-9H-isothiazolo[5,4-b]quinoline-3,4-dione

Conditions
ConditionsYield
Multi-step reaction with 10 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 20 °C
5.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
5.2: 4.70 g / hexane; tetrahydrofuran; CH2Cl2 / -78 - 10 °C
6.1: sodium hydride / dimethylformamide / 0 - 20 °C
6.2: 76 percent / dimethylformamide / 24 h / 20 °C
7.1: sodium hydride / dimethylformamide / 72 h / 75 °C
8.1: 290.9 mg / m-chloroperbenzoic acid / CH2Cl2 / 1 h / 20 °C
9.1: sodium hydrosulfide / dimethylformamide / 1 h / 50 °C
10.1: 121.9 g / aq. NaHCO3; hydroxylamine-O-sulfonic acid / tetrahydrofuran / 2.5 h / 20 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

ethyl 7-bromo-1-cyclopropyl-8-methoxy-2-methylsulfanyl-4-oxo-1,4-dihydroquinoline-3-carboxylate
846563-98-2

ethyl 7-bromo-1-cyclopropyl-8-methoxy-2-methylsulfanyl-4-oxo-1,4-dihydroquinoline-3-carboxylate

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 20 °C
5.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
5.2: 4.70 g / hexane; tetrahydrofuran; CH2Cl2 / -78 - 10 °C
6.1: sodium hydride / dimethylformamide / 0 - 20 °C
6.2: 76 percent / dimethylformamide / 24 h / 20 °C
7.1: sodium hydride / dimethylformamide / 72 h / 75 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

ethyl 7-bromo-1-cyclopropyl-2-mercapto-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate
846564-01-0

ethyl 7-bromo-1-cyclopropyl-2-mercapto-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate

Conditions
ConditionsYield
Multi-step reaction with 9 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 20 °C
5.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
5.2: 4.70 g / hexane; tetrahydrofuran; CH2Cl2 / -78 - 10 °C
6.1: sodium hydride / dimethylformamide / 0 - 20 °C
6.2: 76 percent / dimethylformamide / 24 h / 20 °C
7.1: sodium hydride / dimethylformamide / 72 h / 75 °C
8.1: 290.9 mg / m-chloroperbenzoic acid / CH2Cl2 / 1 h / 20 °C
9.1: sodium hydrosulfide / dimethylformamide / 1 h / 50 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

ethyl 7-bromo-1-cyclopropyl-2-methanesulfinyl-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate
846563-99-3

ethyl 7-bromo-1-cyclopropyl-2-methanesulfinyl-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate

Conditions
ConditionsYield
Multi-step reaction with 8 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 20 °C
5.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
5.2: 4.70 g / hexane; tetrahydrofuran; CH2Cl2 / -78 - 10 °C
6.1: sodium hydride / dimethylformamide / 0 - 20 °C
6.2: 76 percent / dimethylformamide / 24 h / 20 °C
7.1: sodium hydride / dimethylformamide / 72 h / 75 °C
8.1: 290.9 mg / m-chloroperbenzoic acid / CH2Cl2 / 1 h / 20 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

ethyl 2-(4-bromo-2-fluoro-3-methoxybenzoyl)-3-cyclopropylamino-3-methylsulfanylacrylate

ethyl 2-(4-bromo-2-fluoro-3-methoxybenzoyl)-3-cyclopropylamino-3-methylsulfanylacrylate

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1.1: H2 / Pd/C / methanol / 27 h / 20 °C
2.1: aq. HBr; NaNO2 / 0 - 5 °C
2.2: CuBr; aq. HBr / 60 °C
3.1: LDA / tetrahydrofuran; hexane / 1.5 h / -78 °C
3.2: tetrahydrofuran; hexane / -78 - 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 20 °C
5.1: n-BuLi / hexane; tetrahydrofuran / -78 °C
5.2: 4.70 g / hexane; tetrahydrofuran; CH2Cl2 / -78 - 10 °C
6.1: sodium hydride / dimethylformamide / 0 - 20 °C
6.2: 76 percent / dimethylformamide / 24 h / 20 °C
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

3-fluorosalicylaldehyde
394-50-3

3-fluorosalicylaldehyde

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 94 percent / hydrogen / 5percent Pd/C / ethyl acetate / 24 h
3: 84 percent / 48percent HBr / 4.5 h / Heating
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

fluoro-3 methoxy-2 benzaldehhyde
74266-68-5

fluoro-3 methoxy-2 benzaldehhyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 94 percent / hydrogen / 5percent Pd/C / ethyl acetate / 24 h
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

1,3-difluoro-2-methoxybenzene
437-82-1

1,3-difluoro-2-methoxybenzene

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

1,3-difluoro-2-methoxy-5-nitrobenzene
392-25-6

1,3-difluoro-2-methoxy-5-nitrobenzene

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
3: concentrated H2SO4; HNO3
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

3,5-difluoro-4-methoxyaniline
363-47-3

3,5-difluoro-4-methoxyaniline

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
3: concentrated H2SO4; HNO3
4: platinum; methanol / Hydrogenation
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

3,5-difluoro-4-methoxyphenol
443-42-5

3,5-difluoro-4-methoxyphenol

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
3: concentrated H2SO4; HNO3
4: platinum; methanol / Hydrogenation
5: aqueous H2SO4; aqueous CuSO4-solution; xylene / Diazotization
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

4-nitro-benzoic acid-(3-fluoro-2-methoxy-anilide)
345-47-1

4-nitro-benzoic acid-(3-fluoro-2-methoxy-anilide)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: platinum / Hydrogenation
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

4-nitro-benzoic acid-(3,5-difluoro-4-methoxy-anilide)
363-48-4

4-nitro-benzoic acid-(3,5-difluoro-4-methoxy-anilide)

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
3: concentrated H2SO4; HNO3
4: platinum; methanol / Hydrogenation
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

5-(2,6-diiodo-4-nitro-phenoxy)-1,3-difluoro-2-methoxy-benzene
348-92-5

5-(2,6-diiodo-4-nitro-phenoxy)-1,3-difluoro-2-methoxy-benzene

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
3: concentrated H2SO4; HNO3
4: platinum; methanol / Hydrogenation
5: aqueous H2SO4; aqueous CuSO4-solution; xylene / Diazotization
6: K2CO3; pentanone-(2)
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

4,4'-dimethoxy-3,3',5,5'-tetrafluoroazoxybenzene
499-43-4

4,4'-dimethoxy-3,3',5,5'-tetrafluoroazoxybenzene

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
3: concentrated H2SO4; HNO3
4: platinum; methanol / Hydrogenation
View Scheme
1-fluoro-2-methoxy-3-nitrobenzene
484-94-6

1-fluoro-2-methoxy-3-nitrobenzene

4-(3,5-difluoro-4-methoxy-phenoxy)-3,5-diiodo-aniline; hydrochloride
400-84-0

4-(3,5-difluoro-4-methoxy-phenoxy)-3,5-diiodo-aniline; hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1: platinum / Hydrogenation
2: concentrated aqueous HCl / Diazotization.anschliessende Behandlung mit NaBF4 und Erhitzen des erhaltenen Diazonium-tetrafluoroborats unter vermindertem Druck
3: concentrated H2SO4; HNO3
4: platinum; methanol / Hydrogenation
5: aqueous H2SO4; aqueous CuSO4-solution; xylene / Diazotization
6: K2CO3; pentanone-(2)
7: tin (II)-chloride; acetic acid
View Scheme

2-Fluoro-6-nitroanisole Specification

The 2-Fluoro-6-nitroanisole, with the CAS registry number 484-94-6, has the systematic name of 1-fluoro-2-methoxy-3-nitrobenzene. It is a kind of organics, and should be stored in the dry and cool environment. And the molecular formula of this chemical is C7H6FNO3.

The physical properties of 2-Fluoro-6-nitroanisole are as following: (1)ACD/LogP: 1.63; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.63; (4)ACD/LogD (pH 7.4): 1.63; (5)ACD/BCF (pH 5.5): 10.23; (6)ACD/BCF (pH 7.4): 10.23; (7)ACD/KOC (pH 5.5): 183.92; (8)ACD/KOC (pH 7.4): 183.92; (9)#H bond acceptors: 4; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 55.05 Å2; (13)Index of Refraction: 1.521; (14)Molar Refractivity: 39.47 cm3; (15)Molar Volume: 129.4 cm3; (16)Polarizability: 15.64×10-24cm3; (17)Surface Tension: 40.4 dyne/cm; (18)Density: 1.321 g/cm3; (19)Flash Point: 114.9 °C; (20)nthalpy of Vaporization: 48.41 kJ/mol; (21)Boiling Point: 266.4 °C at 760 mmHg; (22)Vapour Pressure: 0.0142 mmHg at 25°C. 

You can still convert the following datas into molecular structure:
(1)SMILES: Fc1cccc([N+]([O-])=O)c1OC
(2)InChI: InChI=1/C7H6FNO3/c1-12-7-5(8)3-2-4-6(7)9(10)11/h2-4H,1H3
(3)InChIKey: RVPBBFKWSJLAPD-UHFFFAOYAN

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