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2-(Bromomethyl)naphthalene

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2-(Bromomethyl)naphthalene Basic information

Product Name:
2-(Bromomethyl)naphthalene
Synonyms:
  • 2-(BROMOMETHYL)NAPHTHALENE
  • 2-BMN
  • BROMOMETHYLNAPTHALENE-2
  • 2-Bromomethylnaphthalene98%
  • 2-(Bromomethyl)naphthalene,96%
  • (2-Naphtylmethyl) bromide
  • Naphthalene, 2-(bromomethyl)-
  • 2-naphthylmethyl bromide
CAS:
939-26-4
MF:
C11H9Br
MW:
221.09
EINECS:
213-359-5
Product Categories:
  • Naphthalene series
  • Aryl
  • Naphthalene derivatives
  • C9 to C12
  • Halogenated Hydrocarbons
Mol File:
939-26-4.mol
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2-(Bromomethyl)naphthalene Chemical Properties

Melting point:
51-54 °C(lit.)
Boiling point:
213 °C100 mm Hg(lit.)
Density 
1.3971 (rough estimate)
refractive index 
1.6411 (estimate)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Chloroform (Sparingly), Ethyl Acetate (Very Slightly)
form 
Fine Crystalline Powder
color 
Slightly yellow to light beige
Water Solubility 
Soluble in water (reacts), and chloroform.
BRN 
636546
CAS DataBase Reference
939-26-4(CAS DataBase Reference)
NIST Chemistry Reference
Naphthalene, 2-(bromomethyl)-(939-26-4)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
34-43-36/37/38-36
Safety Statements 
26-28-36/37/39-45-37-27
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
10-21
Hazard Note 
Corrosive/Keep Cold
HazardClass 
8
PackingGroup 
II
HS Code 
29033036

MSDS

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2-(Bromomethyl)naphthalene Usage And Synthesis

Chemical Properties

White to cream solid

Uses

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Uses

2-(Bromomethyl)naphthalene (2-BMN) can be employed as a starting material in the synthesis of 2-(fluoromethyl)naphthalene , 2-naphthylmethyl azide , 2-naphthalenecarboxaldehyde , diselenide, bis(2-naphthalenylmethyl) , 1H-1,2,3-triazole, 4,4′-(1,4-phenylene)bis[1-(2-naphthalenylmethyl).

Purification Methods

Dissolve the bromo compound in toluene, wash it with saturated aqueous NaHCO3, dry (Mg SO4), evaporate, fractionally distil the residue and recrystallise the solidified distillate from EtOH. [Chapman & Williams J Chem Soc 5044, 1952, Bergmann & Szmuszkovicz Bull Soc Chim Fr 20 566 1953, Beilstein 5 IV 1698.]

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