1,2,3,4-Tetrahydro-1-naphthol

1,2,3,4-Tetrahydro-1-naphthol Basic information
Product Name:1,2,3,4-Tetrahydro-1-naphthol
Synonyms: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;(S)-Tetralin-1-ol;(S)-Tetralin-1β-ol;1-Tetralinol
CAS:529-33-9
MF:C10H12O
MW:148.2
EINECS:208-459-0
Product Categories:Building Blocks;C9 to C20+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Phenols
Mol File:529-33-9.mol
1,2,3,4-Tetrahydro-1-naphthol Structure
1,2,3,4-Tetrahydro-1-naphthol Chemical Properties
Melting point 28-32 °C
Boiling point 102-104 °C2 mm Hg(lit.)
density 1.09 g/mL at 25 °C(lit.)
refractive index n20/D 1.564(lit.)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
solubility 5.09g/l
pka14.33±0.20(Predicted)
form powder to lump to clear liquid
color White or Colorless to Light yellow
Specific Gravity1.090
BRN 2046227
LogP1.980
CAS DataBase Reference529-33-9(CAS DataBase Reference)
NIST Chemistry Reference1-Naphthalenol, 1,2,3,4-tetrahydro-(529-33-9)
EPA Substance Registry System1-Naphthalenol, 1,2,3,4-tetrahydro- (529-33-9)
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38
Safety Statements 22-24/25-37/39-26
WGK Germany 3
RTECS QL5075000
HS Code 29062900
MSDS Information
ProviderLanguage
alpha-Tetralol English
ACROS English
SigmaAldrich English
1,2,3,4-Tetrahydro-1-naphthol Usage And Synthesis
Chemical Propertiesclear colourless to slightly brown viscous liquid
Uses1,2,3,4-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.
1-Naphthol 1,1'-Bi-2-naphthol Adriamycin Tetracycline hydrochloride Tetrahydro TETRAHYDRONAPHTHOL (R)-(-)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL, 9 9% (99% EE/HPLC),(R)-(-)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL p-Naphtholbenzein 6ALPHA-HYDROXYESTRADIOL 1,2,3,4-Tetrahydronaphthalene Terbinafine hydrochloride 1,2,3,4-TETRAHYDRO-1,5-NAPHTHALENEDIOL 4-EPIOXYTETRACYCLINE Phenmedipham (S)-(+)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL, 9 9% (99% EE/HPLC),(S)-(+)-1,2,3,4-TETRAHYDRO-1-NAPHTHOL Chlortetracycline hydrochloride Diethylstilbestrol 1,2,3,4-Tetrahydro-1-naphthol

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