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Factory supply 2-CHLORO-6-NITROPHENOL 603-86-1 with low price

  • Molecular Formula: C6H4ClNO3
  • Molecular Weight: 173.556
  • Appearance/Colour: yellow crystalline powder 
  • Vapor Pressure: 0.0908mmHg at 25°C 
  • Melting Point: 67-71 °C 
  • Refractive Index: 1.5810 (estimate) 
  • Boiling Point: 217.3 °C at 760 mmHg 
  • PKA: 5.43±0.24(Predicted) 
  • Flash Point: 85.2 °C 
  • PSA: 66.05000 
  • Density: 1.554 g/cm3 
  • LogP: 2.47700 

2-CHLORO-6-NITROPHENOL(Cas 603-86-1) Usage

InChI:InChI=1/C6H4ClNO3/c7-4-2-1-3-5(6(4)9)8(10)11/h1-3,9H/p-1

603-86-1 Relevant articles

Preparation method of Eltrombopag

-

Paragraph 0013; 0014, (2018/04/28)

The invention discloses a preparation me...

A ortho-nitro phenol and its derivative synthesis method (by machine translation)

-

, (2017/08/23)

The invention relates to a method for th...

Tertiary Butyl Nitrite Triggered Nitration of Phenols: Solvent- and Structure-Dependent Kinetic Study

Kumar, M. Satish,Rajanna,Venkateswarlu,Rao, K. Lakshman

supporting information, p. 171 - 196 (2016/04/09)

Nitration of phenols with tertiary butyl...

An ortho-nitro phenol synthetic method of compound

-

, (2016/10/10)

The invention relates to a synthesis met...

603-86-1 Process route

2-monochlorophenol
95-57-8

2-monochlorophenol

2-chloro-4-nitrophenol
619-08-9

2-chloro-4-nitrophenol

2-chloro-6-nitrophenol
603-86-1

2-chloro-6-nitrophenol

Conditions
Conditions Yield
With silica supported Al(NO3)3*9H2O; In acetone; at 20 ℃; for 0.416667h; regioselective reaction;
92%
4%
With sodium acetate; acetic acid; sodium nitrite; In water; for 3h; Ambient temperature;
7%
90%
With tert.-butylnitrite; In acetonitrile; at 29.84 ℃; Solvent; Temperature; Kinetics;
88%
With ferric nitrate; 1,3-di-n-butyl-imidazolium tetrafluoroborate; at 30 ℃; for 1h;
78%
15%
With Montmorillonite KSF; nitric acid; hafnium oxychloride; In tetrahydrofuran; at 20 ℃; for 4h;
62%
35%
With ferric nitrate; In ethanol; at 40 ℃; for 2h;
35%
56%
With Yb-Mo-modified montmorillonite HKSF; nitric acid; In tetrahydrofuran; at 20 ℃; for 12h;
54%
43%
With Eb-Mo-modified montmorillonite HKSF; nitric acid; In tetrahydrofuran; at 20 ℃; for 12h;
48%
44%
With acetic acid; sodium nitrite; In cyclohexane; water; for 3h; Product distribution; Ambient temperature; variation of organic solvent or acetate buffer;
47%
43%
With acetic acid; sodium nitrite; In cyclohexane; water; for 3h; Ambient temperature;
47%
43%
With bismuth(III) nitrate; at 20 ℃; for 0.0833333h;
42%
35%
With nickel(II) nitrate hexahydrate; In tetrahydrofuran; at 50 ℃; for 4h; Reagent/catalyst; regioselective reaction;
36%
28%
With tetranitromethane; In cyclohexane; at 20 ℃; Product distribution; Quantum yield; Irradiation;
With methanol; nitric acid;
With nitric acid; die beiden Isomeren werden durch die Barytsalze getrennt;
With nitric acid; In acetic anhydride; Title compound not separated from byproducts;
72 % Spectr.
28 % Spectr.
With nitric acid; acetic acid;
With nitric acid; acetic acid;
With nitric acid;
With nitric acid; In acetic anhydride; at -60 ℃; for 0.25h; Title compound not separated from byproducts;
28 % Spectr.
72 % Spectr.
With oxalic acid; silica gel; sodium nitrite; In dichloromethane; at 20 ℃; for 0.333333h; Further Variations:; Reagents; Product distribution;
With tert.-butylnitrite; silica gel; In acetonitrile; at 100 ℃; under 2250.23 Torr; Time; Temperature; Pressure; Overall yield = 98 %; Microwave irradiation;
3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

2-chloro-4-nitrophenol
619-08-9

2-chloro-4-nitrophenol

p-chloro-o-nitrophenol
89-64-5

p-chloro-o-nitrophenol

2-chloro-6-nitrophenol
603-86-1

2-chloro-6-nitrophenol

Conditions
Conditions Yield
With tert.-butylhydroperoxide; potassium tert-butylate; ammonia; In tetrahydrofuran; for 0.25h;
3%
1%
79%
With potassium hydroxide; oxygen; In ammonia; at -35 - -33 ℃; for 5h; Product distribution; Mechanism;
.66 g
With Cumene hydroperoxide; potassium tert-butylate; In ammonia; at -33 ℃; for 0.25h; Yield given. Yields of byproduct given;

603-86-1 Upstream products

  • 95-57-8
    95-57-8

    2-monochlorophenol

  • 88-73-3
    88-73-3

    2-Chloronitrobenzene

  • 88-75-5
    88-75-5

    2-hydroxynitrobenzene

  • 121-73-3
    121-73-3

    3-Nitrochlorobenzene

603-86-1 Downstream products

  • 946-31-6
    946-31-6

    2-chloro-4,6-dinitro-phenol

  • 38191-33-2
    38191-33-2

    2-amino-6-chlorophenol

  • 80866-77-9
    80866-77-9

    1-chloro-2-methoxy-3-nitro-benzene

  • 59360-18-8
    59360-18-8

    Benzyl-(2-chlor-6-nitrophenyl)-ether

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