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1-Tetralone

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1-Tetralone Basic information

Product Name:
1-Tetralone
Synonyms:
  • KETOTETRAHYDRONAPHTHALENE
  • A-TETRALONE
  • 1,2,3,4-TETRAHYDRO-1-NAPHTHALENONE
  • 1-TETRALONE
  • 3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE
  • 3,4-DIHYDRO-1-(2H)NAPHTHALENEONE
  • 3,4-DIHYDRO-1(2H)-NAPHTHALENONE
  • ALPHA-TETRALONE
CAS:
529-34-0
MF:
C10H10O
MW:
146.19
EINECS:
208-460-6
Product Categories:
  • Bioactive Small Molecules
  • Building Blocks
  • C10
  • Carbonyl Compounds
  • Cell Biology
  • Chemical Synthesis
  • PHARMACEUTICAL INTERMEDIATES
  • Ketones
  • Organic Building Blocks
  • T
  • Cardiovascular & Blood System Agents
  • pharmaceutical
  • bc0001
  • 529-34-0
Mol File:
529-34-0.mol
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1-Tetralone Chemical Properties

Melting point:
2-7 °C(lit.)
Boiling point:
113-116 °C6 mm Hg(lit.)
Density 
1.099 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.568(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Chloroform, Ethyl Acetate (Slightly)
form 
Liquid
color 
brown
Water Solubility 
insoluble
BRN 
607374
InChIKey
XHLHPRDBBAGVEG-UHFFFAOYSA-N
CAS DataBase Reference
529-34-0(CAS DataBase Reference)
NIST Chemistry Reference
1(2H)-Naphthalenone, 3,4-dihydro-(529-34-0)
EPA Substance Registry System
1,2,3,4-Tetrahydronaphthalen-1-one (529-34-0)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-20/22-20/21/22
Safety Statements 
23-24/25-36
WGK Germany 
3
RTECS 
QK4375000
TSCA 
Yes
HS Code 
29143900
Hazardous Substances Data
529-34-0(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 810 mg/kg LD50 dermal Rabbit > 2200 mg/kg

MSDS

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1-Tetralone Usage And Synthesis

Chemical Properties

Clear amber to brown oily liquid

Uses

1-Tetralone is a reagent used in the synthesis of amino-pyrazolopyridines with anti-NF-κB and pro-apoptotic potential.

Synthesis Reference(s)

Tetrahedron Letters, 32, p. 4291, 1991 DOI: 10.1016/S0040-4039(00)92151-8

Purification Methods

Check the IR first. Purify α-tetralone by dissolving 20mL in Et2O (200mL), washing with H2O (100mL), 5% aqueous NaOH (100mL), H2O (100mL), 3% aqueous AcOH (100mL), 5% NaHCO3 (100mL) then H2O (100mL) and dry the ethereal layer over MgSO4. Filter, evaporate and fractionate the residue through a 6in Vigreux column (p 11) under reduced pressure to give a colourless oil (~17g) with b 90-91o/0.50.7mm. [Snyder & Werber Org Synth Coll Vol III 798 1955.] It has also been fractionated through a 0.5metre packed column with a heated jacket under reflux using a partial take-off head. It has max 247.5 and 290nm (hexane). The phenylhydrazone has m 83o. The 2,4,6-trinitrophenylhydrazone has m 247.5-248o (from EtOH). [Olson & Bader Org Synth Coll Vol IV 898 1963, Beilstein 7 H 370, 7 III 1416, 7 IV 1015.]

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