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PENTYLTRIPHENYLPHOSPHONIUM BROMIDE

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PENTYLTRIPHENYLPHOSPHONIUM BROMIDE Basic information

Product Name:
PENTYLTRIPHENYLPHOSPHONIUM BROMIDE
Synonyms:
  • N-PENTYL TRIPHENYLPHOSPHONIUM BROMIDE
  • PENTYLTRIPHENYLPHOSPHONIUM BROMIDE
  • N-AMYL TRIPHENYLPHOSPHONIUM BROMIDE
  • TPL
  • AMYLTRIPHENYLPHOSPHONIUM BROMIDE
  • (1-PENTYL)TRIPHENYLPHOSPHONIUM BROMIDE
  • PENTYLTRIPHENYHLPHOSPHONIUM BROMIDE
  • N-Pentyltriphenylphosphonium bromide, 99+%
CAS:
21406-61-1
MF:
C23H26BrP
MW:
413.33
EINECS:
244-374-5
Product Categories:
  • Phosphonium Compounds
  • Wittig & Horner-Emmons Reaction
  • Wittig Reaction
  • Synthetic Organic Chemistry
Mol File:
21406-61-1.mol
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PENTYLTRIPHENYLPHOSPHONIUM BROMIDE Chemical Properties

Melting point:
165-168 °C
storage temp. 
Inert atmosphere,Room Temperature
form 
solid
color 
White to Almost white
Water Solubility 
Partly miscible in water. Soluble in methanol and chloroform.
Sensitive 
Hygroscopic
BRN 
3580453
InChI
InChI=1S/C23H26P.BrH/c1-2-3-13-20-24(21-14-7-4-8-15-21,22-16-9-5-10-17-22)23-18-11-6-12-19-23;/h4-12,14-19H,2-3,13,20H2,1H3;1H/q+1;/p-1
InChIKey
VAUKWMSXUKODHR-UHFFFAOYSA-M
SMILES
[P+](CCCCC)(C1C=CC=CC=1)(C1C=CC=CC=1)C1=CC=CC=C1.[Br-]
CAS DataBase Reference
21406-61-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-22
Safety Statements 
37/39-26-37
HS Code 
29319090

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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PENTYLTRIPHENYLPHOSPHONIUM BROMIDE Usage And Synthesis

Chemical Properties

LIGHT BROWN TO YELLOW-BROWN CRYSTALLINE POWDER

Uses

It is used as pharmaceutical intermediates.

Synthesis

110-53-2

603-35-0

21406-61-1

General procedure: 1-Bromopentane (1 eq.) was reacted with triphenylphosphine (1.3 eq.) in anhydrous toluene at reflux for 8 to 12 hours under vigorous stirring, referring to literature methods. After completion of the reaction, it was cooled to room temperature and the white solid product was collected by filtration. The solid was washed with excess diethyl ether and subsequently dried. The resulting (1-pentyl)triphenylphosphonium bromide can be used directly in subsequent reactions without further purification.

References

[1] Bulletin de la Societe Chimique de France, 1991, # 3, p. 397 - 406
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985, p. 2307 - 2326
[3] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 19, p. 5168 - 5181
[4] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1996, vol. 35, # 2, p. 99 - 101
[5] Pharmazie, 1999, vol. 54, # 1, p. 26 - 30

PENTYLTRIPHENYLPHOSPHONIUM BROMIDE Preparation Products And Raw materials

Raw materials

PENTYLTRIPHENYLPHOSPHONIUM BROMIDESupplier

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