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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
  • C9 to C12
  • Halogenated Hydrocarbons
  • Naphthalene derivatives
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
InChI
InChI=1S/C11H9Br/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2
InChIKey
RUHJZSZTSCSTCC-UHFFFAOYSA-N
SMILES
C1=C2C(C=CC=C2)=CC=C1CBr
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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