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(4-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE

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(4-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE Basic information

Product Name:
(4-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE
Synonyms:
  • (P-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE
  • (4-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE
  • 4-Chlorobenzyl triphenylphosphonium chloride, 98+%
  • (4-Chlorobenzyl)triphenylphosphonium chloride, min. 95 %
  • (4-Chlorobenzyl)tris(phenyl)phosphonium chloride
  • [(4-Chlorophenyl)methyl]triphenylphosphonium chloride
  • G-KG
  • (4-Chlorobenzyl)triphenylphosphonium Chloride >
CAS:
1530-39-8
MF:
C25H21Cl2P
MW:
423.31
EINECS:
216-228-0
Product Categories:
  • Phosphonium Compounds
  • C-C Bond Formation
  • Olefination
  • Wittig Reagents
Mol File:
1530-39-8.mol
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(4-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE Chemical Properties

Melting point:
>300 °C(lit.)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
almost transparency in Methanol
form 
solid
color 
White to Almost white
Sensitive 
Hygroscopic
BRN 
4173400
CAS DataBase Reference
1530-39-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29319000

MSDS

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(4-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

Reactant for the synthesis of:

  • β-amyloid plaque ligands
  • Selective norbornane-type aspartate analog inhibitors of glutamate transporter 1
  • Pyrethroids with insecticidal activity
  • Chlorinated aromatic avenaciolide analogs with antifungal activity
  • Arylethenylbenzofuroxan derivatives via Wittig-Boden reactions
  • Substituted benzofuroxans for inhibition of Trypanosoma cruzi growth
  • Styrylchromones via Wittig reactions

(4-CHLOROBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDESupplier

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