SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
m-3M3FBS | 200933-14-8 | sc-202217 sc-202217A | 10 mg 50 mg | $141.00 $630.00 | 10 | |
m-3M3FBS functions as a versatile chemical with unique reactivity patterns typical of acid halides. Its electrophilic carbonyl group engages in nucleophilic acyl substitution, allowing for selective reactions with amines and alcohols. The compound's steric hindrance influences reaction kinetics, promoting regioselectivity in synthesis. Additionally, its ability to form stable intermediates enhances its utility in various coupling reactions, showcasing its dynamic role in organic transformations. | ||||||
Spermine, Tetrahydrochloride | 306-67-2 | sc-202817 | 5 g | $166.00 | ||
Spermine, Tetrahydrochloride exhibits distinctive reactivity as a polyamine, characterized by its ability to form strong ionic interactions with negatively charged biomolecules. This compound facilitates complexation with nucleic acids, influencing their structural stability and function. Its multiple amine groups contribute to unique solubility properties, enhancing its role in modulating cellular environments. The compound's high charge density also promotes specific binding affinities, impacting various biochemical pathways. | ||||||
Pseudolaric acid B | 82508-31-4 | sc-203221 sc-203221A | 100 µg 1 mg | $29.00 $74.00 | ||
Pseudolaric acid B is notable for its unique ability to interact with cellular membranes, influencing lipid bilayer dynamics. This compound exhibits distinct hydrophobic characteristics, allowing it to integrate into lipid structures and alter membrane fluidity. Its specific molecular interactions can disrupt protein-lipid associations, potentially affecting signal transduction pathways. Additionally, Pseudolaric acid B's reactivity with various functional groups enhances its role in modulating cellular processes through intricate biochemical mechanisms. | ||||||