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1-BROMO-2-METHYLNAPHTHALENE

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1-BROMO-2-METHYLNAPHTHALENE Basic information

Product Name:
1-BROMO-2-METHYLNAPHTHALENE
Synonyms:
  • 2-Methyl-1-bromonaphthalene
  • beta-Methyl-alpha-bromonaphthalene
  • 1-BROMO-2-METHYLNAPHTHALENE
  • 1-BroMo-2-Methylnaphthalene, GC 90%
  • 1-broMo-2-Methylphthalene
  • 1-BroMo-2-Methylnaphthalene technical grade, 90%
  • 1-Bromo-2-methylnaphtalene
  • 1-BROMO-2-METHYLNAPHTHALENE, TECH., 90%
CAS:
2586-62-1
MF:
C11H9Br
MW:
221.09
EINECS:
219-966-1
Product Categories:
  • Aryl
  • C9 to C12
  • Naphthalene derivatives
  • Halogenated Hydrocarbons
  • Building Blocks
  • C9 to C12
  • Chemical Synthesis
  • Halogenated Hydrocarbons
  • Organic Building Blocks
Mol File:
2586-62-1.mol
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1-BROMO-2-METHYLNAPHTHALENE Chemical Properties

Boiling point:
296 °C (lit.)
Density 
1.418 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.648(lit.)
Flash point:
>230 °F
storage temp. 
Inert atmosphere,Room Temperature
form 
Liquid
color 
Clear yellow
Water Solubility 
Not miscible in water.
BRN 
2042531
CAS DataBase Reference
2586-62-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-11
Safety Statements 
26-36-24/25
WGK Germany 
3
HS Code 
29039990

MSDS

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1-BROMO-2-METHYLNAPHTHALENE Usage And Synthesis

Chemical Properties

CLEAR YELLOW LIQUID

Uses

1-Bromo-2-methylnaphthalene is used as test compound in determination of halogenated hydrocarbons at trace levels by supercritical fluid chromatography-microwave-induced plasma mass spectrometry. Dynamic phosphorescence quenching of 1-bromo-2-methylnaphthalene without deoxygenation has been used for selective sensing of Cu(II) at ngm levels.

Uses

1-Bromo-2-methylnaphthalene was used as test compound in determination of halogenated hydrocarbons at trace levels by supercritical fluid chromatography-microwave-induced plasma mass spectrometry.

General Description

Dynamic phosphorescence quenching of 1-bromo-2-methylnaphthalene without deoxygenation has been used for selective sensing of Cu(II) at ngml-1 levels. It undergoes asymmetric cross-coupling reaction with its corresponding Grignard reagent using a nickel catalyst to form non-racemic 2,2′-dimethyl-1,1′-binaphthyl.

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