1530-42-3

Basic information

• Product Name: Phosphonium,[(4-nitrophenyl)methyl]triphenyl-, chloride (1:1)
• Synonyms: (p-Nitrobenzyl)triphenylphosphoniumchloride (7CI); Phosphonium, (p-nitrobenzyl)triphenyl-, chloride (8CI); Phosphonium, [(4-nitrophenyl)methyl]triphenyl-, chloride (9CI); 4-Nitrobenzyl(triphenyl)phosphonium chloride; NSC 116691; Triphenyl(4-nitrobenzyl)phosphonium chloride
• CAS NO: 1530-42-3
• Molecular Formula: C₂₅H₂₁NO₂P*Cl
• Molecular Weight: 398.413
• Mol File: 1530-42-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• CAS DataBase Reference: Phosphonium,[(4-nitrophenyl)methyl]triphenyl-, chloride (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonium,[(4-nitrophenyl)methyl]triphenyl-, chloride (1:1)(1530-42-3)
• EPA Substance Registry System: Phosphonium,[(4-nitrophenyl)methyl]triphenyl-, chloride (1:1)(1530-42-3)

Safety Data

• Hazardous Substances Data: 1530-42-3(Hazardous Substances Data)

Upstream product

• 100-14-1 4-nitrobenzyl chloride 
• 603-35-0 triphenylphosphine 

Downstream Products

• 1879-55-6 (E)-1-nitro-4-(prop-1-en-1-yl)benzene 
• 1879-54-5 (Z)-p-nitro-(1-propenyl)benzene 
• 4648-33-3 (E)-1-methoxy-4-(4-nitrostyryl)benzene 
• 4648-14-0 (Z)-1-methoxy-4-[2-(4-nitrophenyl)ethenyl]benzene 
• 75840-83-4 5-[(Z)-2-(4-Nitro-phenyl)-vinyl]-1H-imidazole 
• 75840-84-5 5-[(E)-2-(4-Nitro-phenyl)-vinyl]-1H-imidazole 
• 99-99-0 1-methyl-4-nitrobenzene 
• 736-31-2 trans-4,4'-dinitrostilbene 
• 142677-07-4 4-(2-(4-nitrophenyl)ethenyl)-N,N-diphenylaniline 
• 160714-44-3 4-(2-(4-aminophenyl)ethenyl)-N,N-diphenylaniline 
• 62103-05-3 3-(4-methoxy-phenyl)-4-(4-nitro-trans-styryl)-sydnone 
• 62103-04-2 3-(4-methoxy-phenyl)-4-(4-nitro-cis-styryl)-sydnone 
• 62102-97-0 3-methyl-4-(4-nitro-trans-styryl)-sydnone 
• 62102-96-9 3-methyl-4-(4-nitro-cis-styryl)-sydnone 

Relevant articles and documents

Ionic Liquids as Solvents for SN2 Processes. Demonstration of the Complex Interplay of Interactions Resulting in the Observed Solvent Effects

Bimolecular nucleophilic substitution reactions between triphenylphosphine and benzylic electrophiles have been examined in an ionic liquid to probe interactions with species along the reaction coordinate. Trends in the rate constant were found on both varying the leaving group and the electronic nature of the aromatic ring. In all the cases considered, interactions between the components of the ionic liquid and the transition state were shown to be more significant in determining reaction outcome than previously observed for this class of reaction. This demonstrates the importance of considering interactions of the ionic liquid components with all species along the reaction coordinate when investigating the origin of ionic liquid solvent effects, along with how such effects might be exploited.

Substituted diphenyl derivatives

Triazene-substituted diphenyl derivatives are suitable as chemotherapeutic agents for treating carcinomas in humans and animals.

Target directed chemotherapy of tumours of the sexual organs

The invention relates to dialkyltriazene-bearing estrogens and anti-estrogens that are suited for use as chemotherapeutic drugs for treating carcinomas of the sexual organs of humans and animals.