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1-PHENYLNAPHTHALENE

Basic information Synthesis Safety Supplier Related

1-PHENYLNAPHTHALENE Basic information

Product Name:
1-PHENYLNAPHTHALENE
Synonyms:
  • 1-PHENYLNAPHTHALENE
  • 1-naphthylbenzene
  • α-Phenylnaphthalene
  • 1-Phenylnaphthalene,96%
  • 1-Phenylnaphthalene 100mg [605-02-7]
  • 1-Phenylnaphthalene,97%
  • 1-Phenylnaphthalene 96%
  • 1-Phenylnaphthalene@50 μg/mL in Toluene
CAS:
605-02-7
MF:
C16H12
MW:
204.27
EINECS:
210-081-6
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Arenes
  • Building Blocks
  • Organic Building Blocks
  • Organic Building Blocks
Mol File:
605-02-7.mol
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1-PHENYLNAPHTHALENE Chemical Properties

Melting point:
45°C
Boiling point:
324-325 °C (lit.)
Density 
1.085 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.664(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Light orange to Yellow to Green
BRN 
1906885
CAS DataBase Reference
605-02-7(CAS DataBase Reference)
EPA Substance Registry System
1-Phenylnaphthalene (605-02-7)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
2902.90.9000

MSDS

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1-PHENYLNAPHTHALENE Usage And Synthesis

Synthesis


To a suspension of potassium phenyltriflfluoroborate (92.3 mg, 0.5 mmol), 1-bromonapthalene (103.5 mg, 0.5 mmol), and K2CO3 (204.5 mg, 1. 5 mmol) in MeOH  (0.75 mL) was added Pd(OAc)2 in methanol (1.25 mL, 2 × 10–3 M) and then the reaction mixture was stirred and heated at reflflux for 2 h. The mixture was cooled to room temperature and diluted with water (10 mL). The aqueous phase was extracted with CH2Cl2 (3 × 4 mL). The combined organic extracts were washed with brine (10 mL) and dried (MgSO4). The crude product was then purifified via chromatography (silica gel) eluting with hexane to deliver 76.1 mg (75%) of 1-phenylnaphthalene. Reference: Molander, G. A.; Biolatto, B. J. Org. Chem. 2003, 68, 4302−4314.

Chemical Properties

Clear colorless to yellow viscous liquid

Synthesis Reference(s)

Journal of the American Chemical Society, 101, p. 2246, 1979 DOI: 10.1021/ja00502a074
Organic Syntheses, Coll. Vol. 3, p. 729, 1955

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