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(4-BROMOBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE

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(4-BROMOBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE Basic information

Product Name:
(4-BROMOBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE
Synonyms:
  • RARECHEM FH HF 0007
  • (4-BROMOBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE
  • [(4-BROMOPHENYL)METHYL]TRIPHENYLPHOSPHONIUMBROMIDE
  • (4-Bromobenzyl)triphenylphosphonium bromide,97%
  • (4-BroMobenzyl)triphenylphosph
  • (p-Bromobenzyl)triphenylphosphonium bromide
  • (p-Bromob
  • Phosphonium,[(4-?bromophenyl)?methyl]?triphenyl-?,bromide(1:1)
CAS:
51044-13-4
MF:
C25H21Br2P
MW:
512.22
Mol File:
51044-13-4.mol
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(4-BROMOBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE Chemical Properties

Melting point:
270-273 °C
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
solid
color 
White to Almost white
Sensitive 
Hygroscopic
BRN 
4173386
CAS DataBase Reference
51044-13-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
HS Code 
2931.90.6000

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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(4-BROMOBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE Usage And Synthesis

Chemical Properties

cream crystalline powder

Uses

(4-Bromobenzyl)triphenylphosphonium Bromide is used in the preparation of potential precursors for single isomers of buckybowls and carbon nanotubes.

Synthesis

589-15-1

603-35-0

51044-13-4

The reaction was carried out with 4-bromobenzyl bromide (50 g, 200 mmol, 1.0 eq.) and triphenylphosphine (57 g, 220 mmol, 1.1 eq.) in chloroform (400 mL, 0.5 M) at reflux for 4 hours. After completion of the reaction, the reaction solution was cooled to room temperature and ether (1.5 L) was added to precipitate the phosphonium salt. The crude product was dissolved in dichloromethane (300 mL) and precipitated by adding ether (1.5 L) again. It was filtered through a Brinell funnel and washed with ether (500 mL) to give (4-bromobenzyl)triphenylphosphonium bromide (44) as a white solid (123 g, quantitative yield).

References

[1] Patent: WO2005/97812, 2005, A1. Location in patent: Page/Page column 64
[2] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 8, p. 902 - 907
[3] Patent: KR2015/103967, 2015, A. Location in patent: Paragraph 0100
[4] Dyes and Pigments, 2019, vol. 162, p. 959 - 966
[5] Patent: US2008/81934, 2008, A1. Location in patent: Page/Page column 34

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