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(4-Chlorobenzyl)triphenylphosphonium chloride_Molecular_structure_CAS_1530-39-8)
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(4-Chlorobenzyl)triphenylphosphonium chloride

Catalog No. 424587 Name Sigma Aldrich
CAS Number 1530-39-8 Website http://www.sigmaaldrich.com
M. F. C25H21Cl2P Telephone 1-800-521-8956
M. W. 423.314001 Fax
Purity 98% Email
Storage Chembase ID: 82250

SYNONYMS

Title
(4-氯苄基)三苯基氯化磷
IUPAC name
[(4-chlorophenyl)methyl]triphenylphosphanium chloride
IUPAC Traditional name
[(4-chlorophenyl)methyl]triphenylphosphanium chloride
Synonyms
[(4-Chlorophenyl)methyl]triphenylphosphonium chloride

DATABASE IDS

PubChem SID 24866578
MDL Number MFCD00041533
EC Number 216-228-0
CAS Number 1530-39-8

PROPERTIES

Linear Formula ClC6H4CH2P(C6H5)3Cl
Purity 98%
Melting Point >300 °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
5 g in glass bottle
Application
Reactant for the synthesis of:
• β-amyloid plaque ligands1
• Selective norbornane-type aspartate analog inhibitors of glutamate transporter 12
• Pyrethroids with insecticidal activity3
• Chlorinated aromatic avenaciolide analogs with antifungal activity4
• Arylethenylbenzofuroxan derivatives via Wittig-Boden reactions5
• Substituted benzofuroxans for inhibition of Trypanosoma cruzi growth6
• Styrylchromones via Wittig reactions7
Description (简体中文)
包装
5 g in glass bottle
Application
Reactant for the synthesis of:
• β-amyloid plaque ligands1
• Selective norbornane-type aspartate analog inhibitors of glutamate transporter 12
• Pyrethroids with insecticidal activity3
• Chlorinated aromatic avenaciolide analogs with antifungal activity4
• Arylethenylbenzofuroxan derivatives via Wittig-Boden reactions5
• Substituted benzofuroxans for inhibition of Trypanosoma cruzi growth6
• Styrylchromones via Wittig reactions7

REFERENCES