Pharmaceutical

1,6-Dihydroxynaphthalene

  • CAS: 575-44-0
  • Purity: 99%
  • Chinese factory supply 1,6-Dihydroxynaphthalene 575-44-0 in stock with high standard
Inquiry

Chinese factory supply 1,6-Dihydroxynaphthalene 575-44-0 in stock with high standard

  • Molecular Formula: C10H8O2
  • Molecular Weight: 160.172
  • Appearance/Colour: off-white powder 
  • Vapor Pressure: 3.62E-06mmHg at 25°C 
  • Melting Point: 130-133 °C(lit.) 
  • Refractive Index: 1.725 
  • Boiling Point: 375.352 °C at 760 mmHg 
  • PKA: 9.26±0.40(Predicted) 
  • Flash Point: 193.545 °C 
  • PSA: 40.46000 
  • Density: 1.33 g/cm3 
  • LogP: 2.25100 

1,6-Dihydroxynaphthalene(Cas 575-44-0) Usage

Purification Methods

Crystallise it from *benzene or *benzene/EtOH after treatment with charcoal. [Beilstein 6 IV 6557.]

InChI:InChI=1/C10H8O2/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h1-6,11-12H

575-44-0 Relevant articles

Regioselective hydrolysis of diacetoxynaphthalenes catalyzed by Pseudomonas sp. lipase in an organic solvent

Ciuffreda, Pierangela,Casati, Silvana,Santaniello, Enzo

, p. 317 - 321 (2007/10/03)

Depending on the relative positions of t...

Oxyfunctionalization of Hydrocarbons. 17. Acid-Dependent High Regioselectivity Hydroxylation of Naphthalene with Hydrogen Peroxide Giving 1- or 2-Naphthol

Olah, George A.,Keumi, Takashi,Lecoq, Jean Claud,Fung, Alexander P.,Olah, Judith A.

, p. 6148 - 6151 (2007/10/02)

The acid-catalyzed hydroxylation of naph...

Method for preparing aromatic bischloroformate compositions

-

, (2008/06/13)

Bischloroformate oligomer compositions a...

Bischoloroformate preparation method with phosgene removal and monochloroformate conversion

-

, (2008/06/13)

Aqueous bischloroformates are prepared b...

575-44-0 Process route

5-aminonaphthalene-2-sulfonic acid
119-79-9

5-aminonaphthalene-2-sulfonic acid

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

1,6-dihydroxynaphthalene
575-44-0

1,6-dihydroxynaphthalene

5-amino-2-naphthol
86-97-5

5-amino-2-naphthol

1-amino-naphthalene
134-32-7

1-amino-naphthalene

Conditions
Conditions Yield
at 260 ℃; im Autoklaven;
β-naphthol
135-19-3

β-naphthol

2.6-dihydroxynaphthalene
581-43-1

2.6-dihydroxynaphthalene

1,7-Dihydroxynaphthalene
575-38-2

1,7-Dihydroxynaphthalene

1,6-dihydroxynaphthalene
575-44-0

1,6-dihydroxynaphthalene

2,7-Dihydroxynaphthalene
582-17-2

2,7-Dihydroxynaphthalene

Conditions
Conditions Yield
With dihydrogen peroxide; hydrogen fluoride; antimony pentafluoride; at -40 ℃; for 0.25h; Mechanism; Product distribution;
29%
25.5%
11%
3.5%
With dihydrogen peroxide; hydrogen fluoride; antimony pentafluoride; at -40 ℃; for 0.25h;
29%
11%
3.5%
25.5%

575-44-0 Upstream products

  • 119-79-9
    119-79-9

    5-aminonaphthalene-2-sulfonic acid

  • 871887-69-3
    871887-69-3

    2-amino-5-hydroxy-naphthalene-1-sulfonic acid

  • 86-97-5
    86-97-5

    5-amino-2-naphthol

  • 117-62-4
    117-62-4

    2-amino-1,5-naphthalenedisulfonic acid

575-44-0 Downstream products

  • 61419-02-1
    61419-02-1

    naphthofluorescein

  • 22604-07-5
    22604-07-5

    6-methoxy-1-naphthol

  • 150712-57-5
    150712-57-5

    5-methoxynaphthalen-2-ol

  • 4923-53-9
    4923-53-9

    6-hydroxy-[1,4]naphthoquinone

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