(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol

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Names

[ CAS No. ]:
53732-47-1

[ Name ]:
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol

[Synonym ]:
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol
S-Tetralol
(S)-(+)-α-Tetralol
(S)-1,2,3,4-Tetrahydronaphthalen-1-ol
(1S)-1,2,3,4-Tetrahydronaphthalen-1-ol
MFCD00063006
1-Naphthalenol, 1,2,3,4-tetrahydro-, (1S)-
(1S)-1,2,3,4-Tetrahydro-1-naphthalenol

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
254.8±0.0 °C at 760 mmHg

[ Melting Point ]:
37-39ºC

[ Molecular Formula ]:
C10H12O

[ Molecular Weight ]:
148.202

[ Flash Point ]:
99.9±11.0 °C

[ Exact Mass ]:
148.088821

[ PSA ]:
20.23000

[ LogP ]:
2.05

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.585

[ Storage condition ]:
0-10°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
QL5075000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • UNII:87652943HP
  • 3,4-Dihydronaphthalen-1(2H)-one
  • 1-Naphthalenol
  • dihydronaphthalene
  • (S)-1,2,3,4-tetrahydro-1-naphthylbutyrate
  • 1,2,3,4-Tetrahydronaphthalene
  • vinyl acetate
  • Isopropenyl acetate
  • (S)-O-((4aS-(2α,4aα,5α,8α,8aα))-Octahydro-8,9,9-trimethyl-5,8-methano-2H-1-benzopyran-2-yl)-1-tetralol
  • Acetanisole

DownStream

  • 3,4-Dihydronaphthalen-1(2H)-one
  • UNII:87652943HP
  • R-tetralin amine

Articles

Stereochemical sensitivity of the human UDP-glucuronosyltransferases 2B7 and 2B17.

J. Med. Chem. 49 , 1818-27, (2006)

A set of 28 enantiomers comprising rigid and flexible secondary alcohols was synthesized by the asymmetric Corey-Bakshi-Shibata reduction. The enantiomerically pure alcohols were subjected to enzymati...

Factorizing the role of a critical leucine residue in the binding of substrate to human 20alpha-hydroxysteroid dehydrogenase (AKR1C1): molecular modeling and kinetic studies of the Leu308Val mutant enzyme.

Bioorg. Med. Chem. Lett. 20 , 5274-6, (2010)

A comparison of the structures and kinetic properties of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1) and its mutant enzymes (Leu308Val and Leu308Ala) indicates that Leu308 is a selectivity det...


More Articles

Related Compounds

  • (S)-(+)-1,2,3,4-tetrahydro-1-naphthylamine
  • (1S)-1,2,3,4-Tetrahydro-1-naphthalenamine
  • S-(+)-1,2,3,4-tetrahydro-6,7-dibenzyloxy-N-benzyl-1-methyl-isoquinoline-1-carboxylic acid
  • (S)-1,2,3,4-tetrahydro-1-naphthylbutyrate
  • (S)-1,2,3,4-tetrahydro-1-phenylisoquinoline D-(-)-tartrate
  • (S)-1,2,3,4-tetrahydro-1-phenyl-isoquinoline-2-carboxylic acid
  • Methyl 2-methyl-5-aminobenzoic acid
  • 1-(5-bromo-3-methylpyridin-2-yl)-N-methylmethanamine
  • N-(5-bromopyridin-2-yl)-N-methylacetamide
  • (2S,2'R,5'S)-Lilac aldehyde
  • 3-(4-Fluorophenyl)-1,3-dihydro-1-methyl-2H-indol-2-one
  • 3-Sulfamoylthiophene-2-carboxamide
  • 3-(1,2-Oxazol-3-yl)propanoic acid
  • 3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one
  • Pyrazolylmethyl phenyl ether
  • Ethyl 7-methoxycinnoline-3-carboxylate