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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;
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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