Oxygen Compounds
Items 41 to 43 of 43 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
3-Cyclopentyl-1-propanol | 767-05-5 | sc-231664 | 1 g | $33.00 | ||
3-Cyclopentyl-1-propanol is an intriguing oxygen compound distinguished by its alcohol group, which enables strong hydrogen bonding and influences its solubility profile in various solvents. The cyclopentyl moiety introduces steric hindrance, affecting reaction kinetics and selectivity in nucleophilic substitution reactions. Its unique structure also contributes to distinct physical properties, such as moderate viscosity, which can impact its behavior in chemical processes and formulations. | ||||||
4-Ethylbenzyl alcohol | 768-59-2 | sc-232655 | 1 g | $37.00 | ||
4-Ethylbenzyl alcohol is a notable oxygen compound characterized by its aromatic structure, which enhances its ability to engage in π-π stacking interactions. This feature can influence its reactivity in electrophilic aromatic substitution reactions. The presence of the ethyl group introduces additional steric effects, modifying the compound's reactivity and solubility in organic solvents. Its unique molecular architecture also contributes to its distinct viscosity and surface tension properties, impacting its behavior in various chemical environments. | ||||||
2,4-Diaminophenol dihydrochloride | 137-09-7 | sc-238313 | 25 g | $49.00 | ||
2,4-Diaminophenol dihydrochloride exhibits unique electron-donating properties due to its amino groups, facilitating strong intermolecular hydrogen bonding. This compound can engage in redox reactions, acting as a reducing agent in various chemical processes. Its structural configuration allows for effective π-π stacking interactions, influencing its solubility and stability in different solvents. Additionally, the presence of multiple functional groups enhances its reactivity in electrophilic aromatic substitution reactions. | ||||||