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2,6-Naphthalenediol CAS NO: 581-43-1

2,6-Naphthalenediol CAS NO: 581-43-1

Name:2,6-Naphthalenediol
CAS NO: 581-43-1
EINECS:209-465-6
MF:C10H8O2
MW: 160.17
MP: 223-225?¡ãC(lit.)
BP:375.4¡À15.0 ¡ãC at 760 mmHg
Density:1.3¡À0.1 g/cm3
Appearance:?white powder
Purity: 97% min
Package: 25g, 100g, 500g, bulk package
Application:Organic intermediate

Name:2,6-Naphthalenediol????

CAS?NO:?581-43-1

EINECS:209-465-6

MF:C10H8O2?

MW:?160.169

²Ñ±Ê:?223-225?¡ã°ä(±ô¾±³Ù.)

BP:375.4¡À15.0 ¡ãC at 760 mmHg

Density:1.3¡À0.1 g/cm3

Appearance:?white powder?

Purity:?97% min

Package:?25g, 100g, 500g, bulk package?

Application:Organic intermediate

?

Other?name:

2-Hydroxy-6-naphthol;

2,6-Dihydroxynaphthalene;

Naphthalene-2,6-diol;

phthalene-2,6-diol;

1


2,6-Dihydroxynaphthalene CAS NO: 581-43-1? is a reactive intermediate in the Suzuki coupling reaction. It is used as a building block for organic synthesis and has been shown to undergo hydrogen bonding with sodium salts and amides.?


2,6-Dihydroxynaphthalene CAS NO: 581-43-1 also has analytical applications because it can be used to measure transport properties of organic acids. Rat liver microsomes have been found to metabolize 2,6-dihydroxynaphthalene by oxidation at the p-hydroxybenzoic acid group to form a group p2 metabolite.?


This metabolite has also been identified in the urine of rats treated with 2,6-dihydroxynaphthalene CAS NO: 581-43-1. The structure of this compound was determined using X-ray crystal structures. Intramolecular hydrogen bonding was observed in these compounds and confirmed through an x-ray crystal structure analysis.


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