143325-87-5

Basic information

• Product Name: 2,5-dihydroxy-1,2,3,4-tetrahydronaphthalene
• CAS NO: 143325-87-5
• Molecular Weight: 164.204
• Mol File: 143325-87-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,5-dihydroxy-1,2,3,4-tetrahydronaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-dihydroxy-1,2,3,4-tetrahydronaphthalene(143325-87-5)
• EPA Substance Registry System: 2,5-dihydroxy-1,2,3,4-tetrahydronaphthalene(143325-87-5)

Safety Data

• Hazardous Substances Data: 143325-87-5(Hazardous Substances Data)

Upstream product

• 53568-06-2 8-methoxy-1,2,3,4-tetrahydro-2-naphthol 
• 51927-57-2 2,3-epoxy-5-acetoxy-1,2,3,4-tetrahydronaphthalene 
• 27673-48-9 5,8-dihydro-1-naphthol 
• 143325-88-6 1,2,3,4-tetrahydro-2,8-naphthalenediol 
• 51927-56-1 5,8-dihydro-1-naphthyl acetate 
• 35697-10-0 5-hydroxy-2-tetralone 
• 32940-15-1 5-methoxy-2-tetralone 

Downstream Products

• 1159096-19-1 5-benzyloxy-2-tetralol 

Relevant articles and documents

Tetrahydroxynaphthalene reductase: Catalytic properties of an enzyme involved in reductive asymmetric naphthol dearomatization

In reduced circumstances: Tetrahydroxynaphthalene reductase shows a broad substrate range including alternate phenolic compounds and cyclic ketones. Structural modeling reveals major enzyme-substrate interactions; C-terminal truncation of the enzyme causes an altered substrate preference, in accordance with stabilization of the substrate by the C-terminal carboxylate (see picture). This effect allows the identification of a homologous enzyme. Copyright

THE SYNTHESIS AND IDENTIFICATION OF ISOMERIC PRODUCTS OF ENZYMATIC O-DEMETHYLATION OF THE SYMPATHOMIMETIC TETRAMINOL - trans-3-(2-HYDROXYETHYLAMINO)-5,8-DIMETHOXY-1,2,3,4-TETRAHYDRO-2-NAPHTHOL

The structure of the positional isomers of mono-O-demethylated metabolites (V and VI) of Tetraminol - trans-3-(2-hydroxyethylamino)-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol (XIX) - and the pairs of related derivatives was determined.

Tetrahydronaphthyloxy-aminopropanols and salts thereof

This invention relates to new tetrahydronaphthyloxy-aminopropanols and related compounds of the formula SPC1 And to salts of such compounds, which are useful in coronary diseases.