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Heptyltriphenylphosphonium bromide

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Heptyltriphenylphosphonium bromide Basic information

Product Name:
Heptyltriphenylphosphonium bromide
Synonyms:
  • (1-HEPTYL)TRIPHENYLPHOSPHONIUM BROMIDE
  • HEPTYLTRIPHENYLPHOSPHONIUM BROMIDE
  • TTP
  • N-HEPTYLTRIPHENYLPHOSPHONIUM BROMIDE
  • N-HEPTYL TRIPHENYL PHOSPHONIUMROMIDE
  • N-HEPTYLTRIPHENYLPHOSPHONIUM BROMIDE 98+%
  • (1-Heptyl)triphenylphosphonium bromide, 98+%
  • n-Heptyltriphenylphosphonium bromide,99%
CAS:
13423-48-8
MF:
C25H30BrP
MW:
441.38
EINECS:
236-539-5
Product Categories:
  • Phosphonium Compounds
  • Synthetic Organic Chemistry
  • Wittig & Horner-Emmons Reaction
  • Wittig Reaction
  • C-C Bond Formation
  • Olefination
  • Wittig Reagents
Mol File:
13423-48-8.mol
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Heptyltriphenylphosphonium bromide Chemical Properties

Melting point:
173-176 °C(lit.)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
almost transparency in Methanol
form 
Fine Crystalline Powder
color 
White
Sensitive 
Hygroscopic
BRN 
3580843
CAS DataBase Reference
13423-48-8(CAS DataBase Reference)
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Safety Information

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

MSDS

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Heptyltriphenylphosphonium bromide Usage And Synthesis

Chemical Properties

white fine crystalline powder

Uses

Reactant for:

  • Stereospecific rearrangement of epoxides to quaternary carbaldehydes
  • Synthesis of the male pheromone of two species of termite Zootermopsis
  • Regio- and stereoselective TEMPO oxidation
  • Diastereoselective synthesis of climacostol for antitumor activity
  • Enantioselective synthesis of chiral vinylphosphonate and phosphonate analogs of immunosuppressive agent FTY720
  • Preparation of embelin derivatives with XIAP inhibitory and anticancer activity

Uses

Heptyltriphenylphosphonium Bromide can be used for next Reaction:

  1. Stereospecific rearrangement of epoxides to quaternary carbaldehydes.
  2. Synthesis of the male pheromone of two species of termite Zootermopsis.
  3. Regio- and stereoselective TEMPO oxidation.
  4. Diastereoselective synthesis of climacostol for antitumor activity.
  5. Enantioselective synthesis of chiral vinylphosphonate and phosphonate analogs of immunosuppressive agent FTY720.
  6. Preparation of embelin derivatives with XIAP inhibitory and anticancer activity.

Heptyltriphenylphosphonium bromideSupplier

Creasyn Finechem(Tianjin) Co., Ltd.
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