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Heptyltriphenylphosphonium bromide_Molecular_structure_CAS_13423-48-8)
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Heptyltriphenylphosphonium bromide

Catalog No. 377538 Name Sigma Aldrich
CAS Number 13423-48-8 Website http://www.sigmaaldrich.com
M. F. C25H30BrP Telephone 1-800-521-8956
M. W. 441.383461 Fax
Purity 97% Email
Storage Chembase ID: 111786

SYNONYMS

Title
正庚基三苯基溴化磷
IUPAC name
heptyltriphenylphosphanium bromide
IUPAC Traditional name
heptyltriphenylphosphanium bromide

DATABASE IDS

EC Number 236-539-5
CAS Number 13423-48-8
MDL Number MFCD00050249
PubChem SID 24863510

PROPERTIES

Linear Formula CH3(CH2)6P(C6H5)3Br
Purity 97%
Melting Point 173-176 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
50 g in glass bottle
Application
Reactant for:
• Stereospecific rearrangement of epoxides to quaternary carbaldehydes1
• Synthesis of the male pheromone of two species of termite Zootermopsis2
• Regio- and stereoselective TEMPO oxidation3
• Diastereoselective synthesis of climacostol for antitumor activity4
• Enantioselective synthesis of chiral vinylphosphonate and phosphonate analogs of immunosuppressive agent FTY7205
• Preparation of embelin derivatives with XIAP inhibitory and anticancer activity6
Description (简体中文)
包装
50 g in glass bottle
Application
Reactant for:
• Stereospecific rearrangement of epoxides to quaternary carbaldehydes1
• Synthesis of the male pheromone of two species of termite Zootermopsis2
• Regio- and stereoselective TEMPO oxidation3
• Diastereoselective synthesis of climacostol for antitumor activity4
• Enantioselective synthesis of chiral vinylphosphonate and phosphonate analogs of immunosuppressive agent FTY7205
• Preparation of embelin derivatives with XIAP inhibitory and anticancer activity6

REFERENCES