CAS 89996-00-9
:Phosphonium, (2-aminoethyl)triphenyl-, bromide
Description:
Phosphonium, (2-aminoethyl)triphenyl-, bromide is a quaternary ammonium compound characterized by a central phosphorus atom bonded to three phenyl groups and one 2-aminoethyl group, along with a bromide counterion. This compound typically exhibits properties associated with phosphonium salts, such as high thermal stability and solubility in polar solvents. The presence of the aminoethyl group introduces basicity and potential for hydrogen bonding, which can influence its reactivity and interactions with other molecules. As a quaternary ammonium salt, it is likely to be a cationic species, which can enhance its ability to interact with anionic species or surfaces. Its applications may include use as a phase transfer catalyst, in organic synthesis, or in the development of ionic liquids. Safety data should be consulted for handling and storage, as quaternary ammonium compounds can exhibit varying degrees of toxicity and environmental impact. Overall, the unique structure of this phosphonium compound contributes to its diverse chemical behavior and potential applications in various fields.
Formula:C20H21BrNP
Synonyms:- (2-Aminoethyl)triphenylphosphonium Bromide
- Phosphonium, (2-aminoethyl)triphenyl-, bromide
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Found 4 products.
(2-Aminoethyl)triphenylphosphonium Bromide
CAS:Formula:C20H21BrNPPurity:95%Color and Shape:SolidMolecular weight:386.2652(2-Aminoethyl)triphenylphosphonium bromide
CAS:(2-Aminoethyl)triphenylphosphonium bromidePurity:95%Molecular weight:386.27g/mol(2-Aminoethyl)triphenylphosphonium Bromide
CAS:<p>2-Aminoethyl)triphenylphosphonium Bromide is a brominated analog of the amino acid L-cysteine that has shown biological activities. The conformation of this molecule is stabilized by the hydrobromide group, which prevents it from adopting an unnatural conformation. This compound is also sensitive to radiation and can be used in the study of cyano group reactions. 2-Aminoethyl)triphenylphosphonium Bromide has been shown to have cytotoxic activity against cancer cells due to its ability to inhibit protein synthesis at the ribosome level.</p>Formula:C20H21BrNPPurity:Min. 95%Color and Shape:PowderMolecular weight:386.27 g/mol




