Identification | More | [Name]
1,2,3,4-Tetrahydro-1-naphthol | [CAS]
529-33-9 | [Synonyms]
1,2,3,4-TETRAHYDRO-1-NAPHTHOL 1,2,3,4-TETRAHYDRONAPHTHALEN-1-OL 1-HYDROXYTETRALIN 1-TETRALOL AC-ALPHA-TETRALOL (+/-)-ALPHA-TETRALOL ALPHA-TETRALOL A-TETRALOL 1,2,3,4-tetrahydro-1-naphthaleno 1,2,3,4-Tetrahydro-1-naphthalenol 1,2,3,4-tetrahydro-1-naphtho 1,2,3,4-tetrahydro-1-napthol 1,2,3,4-Tetrahydro-alpha-naphthol 1-Naphthol, 1,2,3,4-tetrahydro- Tetrahydro-1-naphthol Tetralin-1-ol 1,2,3,4-Tetrahydro-a-naphthol (1R)-1,2,3,4-Tetrahydro-1-naphthol (1R)-Tetralin-1-ol (R)-1-Hydroxy-1,2,3,4-tetrahydronaphthalene | [EINECS(EC#)]
208-459-0 | [Molecular Formula]
C10H12O | [MDL Number]
MFCD00001739 | [Molecular Weight]
148.2 | [MOL File]
529-33-9.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . S37/39:Wear suitable gloves and eye/face protection . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
QL5075000
| [HS Code ]
29062900 |
Raw materials And Preparation Products | Back Directory | [Raw materials]
1,2,3,4-Tetrahydronaphthalene-->[1,1'-Binaphthalene]-1,1'(2H,2'H)-diol, 3,3',4,4'-tetrahydro--->1,2,3,4-tetrahydro-1-naphthyl hydroperoxide-->1,2,3,4-TETRAHYDRO-2-NAPHTHOL-->1,2-DIHYDRONAPHTHALENE | [Preparation Products]
Brodifacoum-->Flocoumafen-->Coumatetralyl-->5,6,7,8-Tetrahydronaphthalene-1-carboxylic acid-->8-BROMO-3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE-->(R)-(-)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL-->5,6,7,8-TETRAHYDRO-1-NAPHTHOL-->2,3,4,5-Tetrahydro-1H-benzo[b]azepine-->1,2,3,4-Tetrahydro-1-naphthylamine-->2,3-Dihydro-1,4-naphthoquinone-->(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol |
Hazard Information | Back Directory | [Chemical Properties]
clear colourless to slightly brown viscous liquid | [Uses]
1,2,3,4-Tetrahydro-1-naphthol was used as chiral probe to examine the role of three aromatic residues in enzyme-substrate interactions at the sulfuryl acceptor binding site of aryl sulfotransferase IV enzyme. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 61, p. 1493, 1996 DOI: 10.1021/jo951219c | [General Description]
(R)-(-)-enantiomer of 1,2,3,4-Tetrahydro-1-naphthol is a substrate for aryl sulfotransferase (AST) IV enzyme and (S)-(+)-1,2,3,4-tetrahydro-1-naphthol is a competitive inhibitor of AST IV-catalyzed sulfation of 1-naphthalenemethanol. It is the major urinary metabolite of tetralin. |
Spectrum Detail | Back Directory | [Spectrum Detail]
1,2,3,4-Tetrahydro-1-naphthol(529-33-9)MS 1,2,3,4-Tetrahydro-1-naphthol(529-33-9)1HNMR 1,2,3,4-Tetrahydro-1-naphthol(529-33-9)13CNMR 1,2,3,4-Tetrahydro-1-naphthol(529-33-9)IR1 1,2,3,4-Tetrahydro-1-naphthol(529-33-9)Raman
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