1-(Bromomethyl)naphthalene

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CAS:3163-27-7
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CAS:3163-27-7
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1-(Bromomethyl)naphthalene manufacturers

  • 1-(Bromomthy)Naphthalene
  • 1-(Bromomthy)Naphthalene pictures
  • $15.00 / 1KG
  • 2021-07-13
  • CAS:3163-27-7
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
  • 1-(Bromomthy)Naphthalene
  • 1-(Bromomthy)Naphthalene pictures
  • $15.00 / 1KG
  • 2021-07-09
  • CAS:3163-27-7
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
1-(Bromomethyl)naphthalene Basic information
Product Name:1-(Bromomethyl)naphthalene
Synonyms:Naphthalene, 1-(bromomethyl)-;1-BROMOMETHYL NAPHTHALENE;1-BROMOMETHYL NAPHTHALENE 99.73%;1-(Bromomthy)Naphthalene;1-(Bromomethy)naphthalene;(1-Naphtyl)bromomethane;1-Naphtylmethyl bromide;1-(Bromomethyl)napht
CAS:3163-27-7
MF:C11H9Br
MW:221.09
EINECS:801-817-2
Product Categories:Naphthalene series
Mol File:3163-27-7.mol
1-(Bromomethyl)naphthalene Structure
1-(Bromomethyl)naphthalene Chemical Properties
Melting point 52-55°C
Boiling point 213°C/100mmHg
density 1.44
refractive index 1.6600
storage temp. Inert atmosphere,2-8°C
form Powder
color Off-white
Water Solubility Slightly soluble in water.
λmax292nm(Cyclohexane)(lit.)
CAS DataBase Reference3163-27-7(CAS DataBase Reference)
NIST Chemistry Reference1-(Bromomethyl)naphthalene(3163-27-7)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36
RIDADR 3261
HazardClass 8
PackingGroup II
HS Code 29036990
MSDS Information
1-(Bromomethyl)naphthalene Usage And Synthesis
Chemical PropertiesOff-white powder
UsesIt is employed as a intermediate for organic synthesis and pharmaceutical.
Synthesis
1-Naphthalenemethanol

4780-79-4

1-(Bromomethyl)naphthalene

3163-27-7

The general procedure for the synthesis of 1-bromomethylnaphthalene from 1-naphthalenemethanol: Ethyl α,α-diacetoacetate (0.41 mmol, 1.2 eq.), 1-naphthalenemethanol (0.34 mmol, 1.0 eq.), and triphenylphosphine (0.68 mmol, 2.0 eq.) were added to 3 mL of dichloroethane (DCE) at room temperature and the reaction took place in air. The progress of the reaction was monitored by thin layer chromatography (TLC) during the reaction. Upon completion of the reaction, the reaction was quenched by the addition of 3 mL of water, followed by extraction with ethyl acetate (3 x 3 mL). The organic phases were combined, washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography, and the eluent was petroleum ether or a mixed solvent of petroleum ether and ethyl acetate, and the target product 1-bromomethyl naphthalene was finally obtained.

References[1] Synthetic Communications, 2010, vol. 40, # 11, p. 1646 - 1649
[2] Organic Letters, 2003, vol. 5, # 8, p. 1167 - 1169
[3] Tetrahedron Letters, 2014, vol. 55, # 1, p. 90 - 93
[4] Canadian Journal of Chemistry, 1981, vol. 59, p. 2629 - 2641
[5] Tetrahedron, 2003, vol. 59, # 52, p. 10453 - 10463
Tag:1-(Bromomethyl)naphthalene(3163-27-7) Related Product Information
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