Items 161 to 170 of 214 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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2-Bromo-1-(4-cyclohexylphenyl)ethanone | 99433-28-0 | sc-282950 sc-282950A | 1 g 5 g | $400.00 $1185.00 | ||
2-Bromo-1-(4-cyclohexylphenyl)ethanone, as a ketone, showcases intriguing reactivity stemming from its bromine substituent, which introduces significant steric hindrance and alters electronic distribution. This compound engages in selective nucleophilic attacks, leading to the formation of various adducts. Its bulky cyclohexyl group enhances conformational rigidity, influencing reaction pathways and kinetics. The compound's polar characteristics also play a crucial role in solubility and interaction with solvents, affecting its reactivity in diverse chemical contexts. | ||||||
4-Oxo-2-nonenal | 103560-62-9 | sc-202020 sc-202020A | 1 mg 5 mg | $150.00 $720.00 | ||
4-Oxo-2-nonenal, as a ketone, exhibits notable reactivity due to its conjugated carbonyl group, which enhances electrophilicity and facilitates Michael addition reactions. The presence of the unsaturated chain allows for unique interactions with nucleophiles, promoting diverse reaction pathways. Its structural features contribute to distinct physical properties, such as increased volatility and reactivity with various functional groups, influencing its behavior in complex chemical environments. | ||||||
(R)-(+)-HA-966 | 123931-04-4 | sc-361303 | 5 mg | $95.00 | ||
(R)-(+)-HA-966, as a ketone, showcases intriguing stereochemical properties that influence its reactivity and interaction with other molecules. The chiral center enhances its selectivity in reactions, allowing for specific pathways in synthesis. Its carbonyl group participates in hydrogen bonding, affecting solubility and reactivity with nucleophiles. Additionally, the compound's unique spatial arrangement can lead to distinct kinetic profiles in reactions, making it a subject of interest in mechanistic studies. | ||||||
YM 976 | 191219-80-4 | sc-204411 sc-204411A | 10 mg 50 mg | $207.00 $825.00 | ||
YM 976, classified as a ketone, exhibits notable electronic properties due to its conjugated system, which enhances its reactivity in electrophilic addition reactions. The presence of the carbonyl group allows for significant dipole interactions, influencing its solubility in various solvents. Its unique steric configuration can lead to selective reactivity, facilitating specific pathways in organic transformations. Furthermore, the compound's kinetic behavior is characterized by rapid reaction rates, making it a compelling subject for studies on reaction mechanisms. | ||||||
NBI-31772 | 374620-70-9 | sc-222047A sc-222047 sc-222047B sc-222047C | 1 mg 5 mg 10 mg 25 mg | $39.00 $162.00 $267.00 $573.00 | ||
NBI-31772, a ketone, showcases intriguing photophysical properties, particularly in its ability to engage in intramolecular hydrogen bonding, which stabilizes its structure and influences its reactivity. The compound's unique spatial arrangement allows for selective interactions with nucleophiles, promoting distinct reaction pathways. Additionally, its polar nature enhances solvation dynamics, affecting its behavior in various chemical environments and contributing to its kinetic profile in reactions. | ||||||
FKGK 11 | 1071000-98-0 | sc-223989 sc-223989A | 500 µg 1 mg | $54.00 $136.00 | ||
FKGK 11, classified as a ketone, exhibits remarkable electronic properties due to its conjugated system, which facilitates efficient charge transfer. This compound demonstrates a propensity for forming stable complexes with metal ions, influencing its reactivity and selectivity in catalytic processes. Its unique steric configuration allows for specific interactions with electrophiles, leading to diverse reaction mechanisms. Furthermore, the compound's moderate polarity enhances its solubility in various organic solvents, impacting its behavior in synthetic applications. | ||||||
Mesityl oxide | 141-79-7 | sc-250308 | 100 g | $40.00 | ||
Mesityl oxide, a ketone, features a branched structure that contributes to its unique reactivity profile. Its ability to engage in enolization allows for dynamic equilibrium between keto and enol forms, influencing reaction pathways. The compound's steric hindrance affects its interaction with nucleophiles, leading to selective reactions. Additionally, its moderate volatility and distinct odor can impact its behavior in various chemical environments, making it an interesting subject for study in organic synthesis. | ||||||
Formononetin | 485-72-3 | sc-202614 | 5 mg | $122.00 | 2 | |
Formononetin, a naturally occurring ketone, exhibits intriguing molecular interactions due to its phenolic structure. This compound can participate in hydrogen bonding, enhancing its solubility in polar solvents. Its reactivity is influenced by the presence of electron-donating groups, which can stabilize transition states during reactions. Furthermore, Formononetin's ability to undergo oxidation and reduction reactions highlights its versatility in organic transformations, making it a subject of interest in chemical research. | ||||||
2-Chlorocyclohexanone | 822-87-7 | sc-237997 sc-237997A | 5 g 25 g | $18.00 $88.00 | ||
2-Chlorocyclohexanone is a unique ketone characterized by its chlorinated cyclohexane ring, which introduces distinct steric and electronic effects. The presence of the chlorine atom enhances electrophilicity, facilitating nucleophilic attack in various reactions. Its ring structure allows for conformational flexibility, influencing reaction pathways and kinetics. Additionally, this compound can engage in dipole-dipole interactions, affecting solubility and reactivity in diverse chemical environments. | ||||||
1,4-Bis(acryloyl)piperazine | 6342-17-2 | sc-203424 sc-203424A | 5 g 10 g | $150.00 $260.00 | ||
1,4-Bis(acryloyl)piperazine is a distinctive compound featuring dual acrylamide functionalities that promote unique polymerization behavior. Its piperazine ring contributes to enhanced hydrogen bonding and dipole interactions, influencing reactivity and stability. The acrylate groups facilitate rapid radical polymerization, allowing for tailored material properties. This compound's ability to form cross-linked networks enhances mechanical strength and thermal stability, making it suitable for diverse applications in polymer chemistry. |