CAS 34696-66-7

Benzenemethanaminium,4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-N,N,N-trimethyl-, iodide

Description:

Benzenemethanaminium, 4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-N,N,N-trimethyl-, iodide, with CAS number 34696-66-7, is a quaternary ammonium compound characterized by its trimethylammonium group and a pyrrolidine derivative. This compound typically exhibits properties associated with quaternary ammonium salts, such as being a cationic surfactant, which can enhance solubility in aqueous solutions and facilitate interactions with biological membranes. The presence of the iodide ion contributes to its ionic nature, potentially influencing its reactivity and stability. The pyrrolidine moiety, with its dioxo substituents, may impart specific biological activities, making it of interest in medicinal chemistry. Additionally, such compounds often demonstrate antimicrobial properties and can be utilized in various applications, including drug formulation and as a reagent in organic synthesis. Overall, the unique structural features of this compound suggest potential utility in both pharmaceutical and industrial contexts, although specific applications would depend on further research into its biological activity and chemical behavior.

Formula: C₁₄H₁₇N₂O₂I

4-(N-Maleimido)benzyl-α-trimethylammonium Iodide

Controlled Product

CAS: 34696-66-7

Applications A charged sulfhydryl reactive reagent.
References Karlin, A., et al.: J. Mol. Biol. , 61, 175 (1971)

Formula: C₁₄H₁₇N₂O₂·I

Color and Shape: Neat

Molecular weight: 372.20

Ref: TR-M135000

4-(N-Maleimido)benzyl-a-trimethylammonium iodide

CAS: 34696-66-7

4-(N-Maleimido)benzyl-a-trimethylammonium iodide is a carotenoid that acts as an agonist binding site for the receptor molecule. It has been shown to inhibit tumor cell growth and induce apoptosis. 4-(N-Maleimido)benzyl-a-trimethylammonium iodide binds to the redox potential of iron atoms, which are important in many biochemical reactions and in maintaining iron homeostasis. The x-ray crystal structures of this compound show that it has a chemical biology model system and can be used to study the function of toll-like receptors. This drug also has an irreversible inhibition effect on cation channels, which may be due to its ability to block the opening of these channels by binding to them.

Formula: C₁₄H₁₇IN₂O₂

Purity: Min. 95%

Color and Shape: Yellow Solid

Molecular weight: 372.2 g/mol

Ref: 3D-FM24977