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1,2-DIHYDRONAPHTHALENE

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1,2-DIHYDRONAPHTHALENE Basic information

Product Name:
1,2-DIHYDRONAPHTHALENE
Synonyms:
  • DELTA1-DIALIN
  • 1,2-DIHYDRONAPHTHALENE
  • 1,2-Dialin
  • 1,2-dihydro-naphthalen
  • Dialin
  • Diolin
  • Dihydronaphthalene
  • 1,2-DIHYDRONAPHTHALENE OEKANAL, 250 MG
CAS:
447-53-0
MF:
C10H10
MW:
130.19
EINECS:
207-183-8
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Alpha Sort
  • Analytical Standards
  • AromaticsVolatiles/ Semivolatiles
  • Organic Building Blocks
  • Chemical Class
  • D
  • DAlphabetic
  • DID - DINAnalytical Standards
  • Hydrocarbons
  • NaphthalenesChemical Class
  • NeatsAnalytical Standards
  • PAHsMore...Close...
  • Arenes
  • Building Blocks
  • Organic Building Blocks
Mol File:
447-53-0.mol
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1,2-DIHYDRONAPHTHALENE Chemical Properties

Melting point:
−8 °C(lit.)
Boiling point:
89 °C16 mm Hg(lit.)
Density 
0.997 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.582(lit.)
Flash point:
153 °F
storage temp. 
Sealed in dry,Room Temperature
color 
Colorless to Light yellow
Water Solubility 
Not miscible or difficult to mix with water.
BRN 
1851372
CAS DataBase Reference
447-53-0(CAS DataBase Reference)
EPA Substance Registry System
Naphthalene, 1,2-dihydro- (447-53-0)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
RTECS 
QJ4375000
HS Code 
29029000

MSDS

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1,2-DIHYDRONAPHTHALENE Usage And Synthesis

Chemical Properties

CLEAR LIGHT YELLOW TO SLIGHTLY BROWN LIQUID

Definition

ChEBI: A dihydronaphthalene hydrogenated at C-1 and C-2.

Synthesis Reference(s)

Tetrahedron Letters, 28, p. 2481, 1987 DOI: 10.1016/S0040-4039(00)95446-7

Synthesis

Dissolve 1,2-naphthoquinone (0.18 mmol) in ethanol (3 mL). NaBH4 (73 mg, 1.93 mmol) suspended in ethanol (3 mL) was added dropwise to the reaction mixture. The mixture was stirred at room temperature under nitrogen. After 1.5 hours, the mixture was poured into ice water (50 mL). Acidify the mixture with HCl (0.5 M). The mixture was extracted with CH2Cl2. The mixture was dried over magnesium sulfate. The mixture was concentrated to give 1,2-dihydroxynaphthalene.

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