Alcohols
Items 401 to 410 of 413 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(R)-(−)-1-Phenyl-1,2-ethanediol | 16355-00-3 | sc-253363 | 1 g | $61.00 | ||
(R)-(-)-1-Phenyl-1,2-ethanediol is a chiral alcohol characterized by its phenyl group, which imparts unique steric and electronic properties. This compound engages in hydrogen bonding, enhancing its solubility in polar solvents and influencing its reactivity in various chemical environments. Its stereochemistry allows for selective interactions in asymmetric synthesis, while its ability to participate in oxidation reactions showcases its versatility in organic transformations. | ||||||
2-Butyn-1-ol | 764-01-2 | sc-237962 sc-237962A | 5 g 25 g | $58.00 $197.00 | ||
2-Butyn-1-ol is characterized by its terminal alkyne functional group, which imparts unique reactivity in nucleophilic addition reactions. The presence of the hydroxyl group enhances its ability to participate in hydrogen bonding, influencing solubility and reactivity in various solvents. Its linear structure allows for efficient steric interactions, facilitating specific reaction pathways. Additionally, the compound can undergo dehydration to form alkynes, showcasing its versatility in synthetic transformations. | ||||||
3-Chloro-1-propanol | 627-30-5 | sc-238511 sc-238511A | 25 g 100 g | $32.00 $90.00 | ||
3-Chloro-1-propanol exhibits unique reactivity due to its chloroalkyl group, which can participate in nucleophilic substitution reactions. The presence of the hydroxyl group enhances its ability to form hydrogen bonds, influencing solubility in polar solvents. This compound can also engage in esterification reactions, acting as a versatile intermediate in organic synthesis. Its molecular structure allows for specific steric interactions, affecting reaction pathways and kinetics in various chemical transformations. | ||||||
3-Fluoro-2-hydroxybenzoic acid | 341-27-5 | sc-260911 sc-260911A | 1 g 5 g | $78.00 $316.00 | ||
3-Fluoro-2-hydroxybenzoic acid exhibits intriguing properties as a carboxylic acid, characterized by its ability to form strong hydrogen bonds due to the hydroxyl group. This enhances its solubility in polar solvents and influences its reactivity in esterification and acylation reactions. The presence of the fluorine atom introduces unique electronic effects, modulating acidity and reactivity, which can lead to selective interactions in various chemical environments. | ||||||
α-Terpineol | 98-55-5 | sc-291877 sc-291877B sc-291877C sc-291877A | 25 ml 50 ml 100 ml 500 ml | $51.00 $127.00 $189.00 $246.00 | ||
α-Terpineol is characterized by its unique hydrogen bonding capabilities, which enhance its solubility in various solvents. This compound exhibits a distinct reactivity profile, particularly in electrophilic aromatic substitution reactions, where its hydroxyl group can act as a directing group. Additionally, its chiral nature contributes to diverse stereochemical outcomes in reactions, making it a valuable subject for studying reaction kinetics and molecular interactions in organic synthesis. | ||||||
Acetoin | 513-86-0 | sc-239186 | 25 g | $74.00 | ||
Acetoin, a diketone, exhibits unique reactivity due to its carbonyl groups, which can engage in nucleophilic addition reactions. This compound participates in various condensation reactions, forming diverse derivatives. Its ability to stabilize enol forms enhances its reactivity in electrophilic aromatic substitutions. Additionally, Acetoin's polar nature influences solubility and intermolecular interactions, making it a versatile intermediate in organic synthesis and a key player in metabolic pathways. | ||||||
L-(−)-Glyceric acid hemicalcium salt monohydrate | 6057-35-8 | sc-250210 sc-250210A | 1 g 2 g | $235.00 $420.00 | 1 | |
L-(-)-Glyceric acid hemicalcium salt monohydrate exhibits unique chelation properties, forming stable complexes with metal ions that enhance its reactivity in various biochemical pathways. Its monohydrate form contributes to increased solubility, facilitating efficient molecular interactions in aqueous environments. The compound's ability to participate in hydrogen bonding and ionic interactions further influences its stability and reactivity, making it a key player in specific catalytic processes. | ||||||
Sodium DL-lactate solution | 72-17-3 | sc-301818 sc-301818A sc-301818B | 100 ml 500 ml 1 L | $16.00 $47.00 $85.00 | 2 | |
Sodium DL-lactate solution is a versatile compound featuring a chiral lactate ion that participates in various ionic interactions. Its solubility in water enhances its reactivity, allowing it to act as a buffering agent in biochemical systems. The presence of both sodium and lactate ions facilitates unique ion pairing and stabilization of charged species, influencing reaction kinetics. This solution's ability to modulate pH levels and maintain osmotic balance is critical in various chemical environments. | ||||||
1-Ethynyl-1-cyclohexanol | 78-27-3 | sc-237552 | 100 ml | $36.00 | ||
1-Ethynyl-1-cyclohexanol exhibits intriguing reactivity due to its terminal alkyne functionality, which can engage in various coupling reactions, including Sonogashira and alkyne metathesis. The steric hindrance from the cyclohexanol moiety influences its reactivity profile, allowing for selective transformations. Its ability to form hydrogen bonds enhances solubility in polar solvents, while the presence of the alkyne introduces unique spectroscopic features, aiding in structural elucidation. | ||||||
3-Iodo-1-propanol | 627-32-7 | sc-231755 | 1 g | $23.00 | ||
3-Iodo-1-propanol is a halogenated alcohol notable for its reactivity in nucleophilic substitution reactions, where the iodine atom serves as a good leaving group. Its molecular structure promotes strong dipole interactions, enhancing solubility in polar solvents. The compound can participate in various coupling reactions, leading to the formation of diverse carbon frameworks. Additionally, it exhibits unique stereochemical properties that can influence reaction pathways and product distributions. | ||||||