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529-33-9,MFCD00001739
Catalog No.:AA003D76

529-33-9 | 1,2,3,4-Tetrahydro-1-naphthol

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Purity
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250mg
97%
in stock  
$8.00   $6.00
- +
1g
97%
in stock  
$11.00   $8.00
- +
5g
98%
in stock  
$29.00   $20.00
- +
25g
95%
in stock  
$44.00   $31.00
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100g
95%
in stock  
$153.00   $108.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003D76
Chemical Name:
1,2,3,4-Tetrahydro-1-naphthol
CAS Number:
529-33-9
Molecular Formula:
C10H12O
Molecular Weight:
148.2017
MDL Number:
MFCD00001739
SMILES:
OC1CCCc2c1cccc2
NSC Number:
5172
Properties
Properties
 
BP:
254.8°C at 760 mmHg  
Form:
Solid  
MP:
28-32 °C  
Refractive Index:
n20/D 1.564(lit.)  
Solubility:
5.09g/l  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
133  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Undefined Atom Stereocenter Count:
2  
XLogP3:
1.8  

Literature

Title: Gold nanoparticles incarcerated in nanoporous syndiotactic polystyrene matrices as new and efficient catalysts for alcohol oxidations.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20120109

Title: Synthesis of novel mast cell-stabilising and anti-allergic 1,2,3,4-tetrahydro-1-naphthalenols and related compounds.

Journal: European journal of medicinal chemistry 20110501

Title: Spectroscopic investigations on Naphthol and Tetrahydronaphthol. A theoretical approach.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110201

Title: To remove or not to remove? The challenge of extracting the template to make the cavities available in Molecularly Imprinted Polymers (MIPs).

Journal: International journal of molecular sciences 20110101

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Antitumor agents 269. Non-aromatic ring-A neotanshinlactone analog, TNO, as a new class of potent antitumor agents.

Journal: Bioorganic & medicinal chemistry letters 20091115

Title: An inner pore residue (Asn406) in the Nav1.5 channel controls slow inactivation and enhances mibefradil block to T-type Ca2+ channel levels.

Journal: Molecular pharmacology 20061101

Title: Monocyclic and dicyclic hydrocarbons: structural requirements for proximal giant axonopathy.

Journal: Acta neuropathologica 20060901

Title: Breakdown products on metabolic pathway of degradation of benz[a]anthracene by a ligninolytic fungus.

Journal: Chemosphere 20060701

Title: Aryltetralol and aryltetralone lignans from Holostylis reniformis.

Journal: Phytochemistry 20060501

Title: Mode of binding of methyl acceptor substrates to the adrenaline-synthesizing enzyme phenylethanolamine N-methyltransferase: implications for catalysis.

Journal: Biochemistry 20051227

Title: Sub- and supercritical chiral separation of racemic compounds on columns with stationary phases having different functional groups.

Journal: Chemical & pharmaceutical bulletin 20051001

Title: Unexpectedly small ortho-oxygen substituent effects on stabilities of benzylic carbocations.

Journal: Journal of the American Chemical Society 20040818

Title: Dopamine-induced death of PC12 cells is prevented by a substituted tetrahydronaphthalene.

Journal: Neuropharmacology 20040601

Title: Influence of phenylalanines 77 and 138 on the stereospecificity of aryl sulfotransferase IV.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20040501

Title: Comparative molecular field analysis of substrates for an aryl sulfotransferase based on catalytic mechanism and protein homology modeling.

Journal: Journal of medicinal chemistry 20021205

Title: Enantioselective routes to both enantiomers of aryl alcohols with a single catalyst antipode: Ru and Os transfer hydrogenation catalysts.

Journal: Organic letters 20011115

Title: Evidence against an action of mibefradil at N-type voltage-operated calcium channels.

Journal: Naunyn-Schmiedeberg's archives of pharmacology 20011101

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Tags:529-33-9 Molecular Formula|529-33-9 MDL|529-33-9 SMILES|529-33-9 1,2,3,4-Tetrahydro-1-naphthol