Items 291 to 300 of 380 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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3-(Trimethylsilyl)-2-propynal | 2975-46-4 | sc-231417 | 1 g | $77.00 | ||
3-(Trimethylsilyl)-2-propynal is a silicon compound distinguished by its unique reactivity profile and molecular structure. The trimethylsilyl group enhances its stability while also acting as a leaving group in nucleophilic substitution reactions. This compound exhibits significant electrophilicity due to the presence of the propynal moiety, promoting rapid reaction kinetics. Its distinct steric and electronic properties influence its behavior in various synthetic pathways, making it a valuable intermediate in organic synthesis. | ||||||
4-[(Trimethylsilyl)ethynyl]morpholine | 64024-63-1 | sc-232347 | 1 g | $72.00 | ||
4-[(Trimethylsilyl)ethynyl]morpholine is a silicon compound characterized by its intriguing molecular architecture and reactivity. The trimethylsilyl group imparts enhanced solubility and stability, facilitating its participation in diverse coupling reactions. Its morpholine ring contributes to unique hydrogen bonding interactions, influencing its reactivity and selectivity in synthetic pathways. This compound's distinctive electronic properties enable it to act as a versatile building block in various chemical transformations. | ||||||
Trimethoxyphenylsilane | 2996-92-1 | sc-251346 sc-251346A | 50 ml 250 ml | $39.00 $91.00 | ||
Trimethoxyphenylsilane is a silicon compound notable for its unique silane functionality, which enhances surface adhesion and promotes cross-linking in polymer matrices. The presence of methoxy groups allows for facile hydrolysis, leading to the formation of silanol species that can engage in condensation reactions. Its phenyl group contributes to π-π stacking interactions, influencing the compound's reactivity and stability in various chemical environments, making it a key player in silane chemistry. | ||||||
2-(4-fluorophenyl)-5-(trimethylsilyl)-1,3,4-oxadiazole | sc-339920 sc-339920A | 250 mg 1 g | $248.00 $510.00 | |||
2-(4-fluorophenyl)-5-(trimethylsilyl)-1,3,4-oxadiazole is a silicon compound characterized by its oxadiazole ring, which imparts unique electronic properties and enhances its reactivity. The trimethylsilyl group increases lipophilicity and stabilizes the molecule against hydrolysis, while the fluorophenyl moiety introduces strong dipole interactions. This combination facilitates selective coordination with metal centers and influences reaction kinetics, making it a versatile component in silicon-based materials. | ||||||
3-(Trimethylsilyloxy)-1-butyne | 17869-76-0 | sc-225917 | 5 g | $32.00 | ||
3-(Trimethylsilyloxy)-1-butyne is a silicon compound notable for its unique reactivity stemming from the trimethylsilyloxy group, which enhances nucleophilicity and promotes efficient coupling reactions. The presence of the alkyne moiety allows for distinct π-π stacking interactions, influencing its behavior in polymerization processes. Additionally, the compound exhibits significant thermal stability, making it suitable for high-temperature applications while maintaining its structural integrity. | ||||||
N-[3-(Trimethylsilyl)-2-propynyl]phthalimide | 351029-12-4 | sc-235978 | 1 g | $59.00 | ||
N-[3-(Trimethylsilyl)-2-propynyl]phthalimide is a silicon compound characterized by its distinctive phthalimide structure, which facilitates strong π-electron interactions. The trimethylsilyl group enhances its electrophilic properties, allowing for rapid reaction kinetics in nucleophilic substitution processes. This compound also exhibits unique solubility characteristics, promoting compatibility with various organic solvents, which can influence its reactivity in synthetic pathways. | ||||||
2-(Trimethylsilyl)phenyl trifluoromethanesulfonate | 88284-48-4 | sc-223306 sc-223306A | 1 g 5 g | $46.00 $138.00 | ||
2-(Trimethylsilyl)phenyl trifluoromethanesulfonate is a silicon compound notable for its triflate moiety, which significantly enhances its reactivity as an electrophile. The presence of the trimethylsilyl group not only stabilizes the molecule but also increases its lipophilicity, facilitating interactions with nucleophiles. This compound exhibits unique selectivity in coupling reactions, making it a versatile intermediate in organic synthesis, particularly in forming carbon-carbon bonds. | ||||||
Trimethylsilyl-D-(+)-mannitol | 14317-07-8 | sc-216012 | 500 mg | $200.00 | ||
Trimethylsilyl-D-(+)-mannitol is a silicon compound characterized by its unique stereochemistry and the presence of a trimethylsilyl group, which enhances its solubility in organic solvents. This compound exhibits distinctive reactivity patterns, particularly in nucleophilic substitution reactions, where the silicon atom can act as a leaving group. Its ability to form stable complexes with various substrates allows for selective transformations, making it an intriguing candidate for exploring silicon-based reactivity in synthetic pathways. | ||||||
Silica Gel, 35-70 Micron Particles | sc-220102 sc-220102A sc-220102B sc-220102C | 1 kg 2.5 kg 5 kg 10 kg | $300.00 $540.00 $1030.00 $1801.00 | |||
Silica gel, composed of 35-70 micron particles, is a highly porous silicon compound known for its exceptional surface area and adsorption properties. Its amorphous structure facilitates strong van der Waals interactions with moisture and organic molecules, enabling efficient desiccation. The material's high thermal stability and inertness contribute to its versatility in various applications, while its ability to undergo physical changes without chemical alteration allows for tailored performance in diverse environments. | ||||||
Silica Gel, 40-63 Micron Particles | 112926-00-8 | sc-220103 | 500 g | $305.00 | ||
Silica gel, featuring 40-63 micron particles, is a versatile silicon compound characterized by its extensive porosity and high surface area. This amorphous material exhibits unique adsorption dynamics, allowing it to selectively interact with a wide range of polar and non-polar substances. Its robust framework enhances mechanical strength, while the intricate pore structure facilitates rapid diffusion of gases and liquids, making it an effective medium for various physical processes. |