Carbonyl Compounds
Items 161 to 170 of 235 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Methyl 2-chloropropionate | 17639-93-9 | sc-228495 | 25 mL | $46.00 | ||
Methyl 2-chloropropionate is a notable carbonyl compound that exhibits unique electrophilic characteristics due to its chlorinated structure. The presence of the chlorine atom enhances its reactivity, facilitating nucleophilic substitution reactions. This compound can engage in acylation processes, leading to the formation of diverse derivatives. Its polar nature contributes to distinct solvation dynamics, influencing reaction kinetics and selectivity in various organic transformations. | ||||||
2-Ethylhexyl chloroformate | 24468-13-1 | sc-225349 | 100 g | $94.00 | ||
2-Ethylhexyl chloroformate is a distinctive carbonyl compound characterized by its ability to act as a potent acylating agent. The chloroformate group enhances its electrophilicity, allowing for rapid reactions with nucleophiles. This compound exhibits unique steric effects due to its branched alkyl chain, which can influence reaction pathways and selectivity. Its reactivity is further modulated by solvent interactions, impacting the kinetics of acylation and esterification processes. | ||||||
Hydroxybutyl methacrylate, mixture of isomers | 29008-35-3 | sc-235337 | 100 g | $99.00 | ||
Hydroxybutyl methacrylate, a mixture of isomers, is a versatile carbonyl compound notable for its dual functionality as both a reactive monomer and a polymerizable agent. Its hydroxyl and methacrylate groups facilitate hydrogen bonding and enhance its reactivity towards nucleophiles. The presence of multiple isomers introduces variability in physical properties, such as viscosity and solubility, which can significantly influence polymerization kinetics and the resulting material characteristics. | ||||||
1-[2-(Trimethylsilyl)ethoxycarbonyloxy]benzotriazole | 113306-55-1 | sc-287050 sc-287050A | 1 g 5 g | $98.00 $420.00 | ||
1-[2-(Trimethylsilyl)ethoxycarbonyloxy]benzotriazole exhibits intriguing properties as a carbonyl compound, particularly through its unique silyl ether functionality. The trimethylsilyl group enhances stability and solubility, facilitating selective nucleophilic attacks. Its benzotriazole moiety contributes to strong π-π interactions, influencing reaction kinetics and pathways. This compound's distinctive structure allows for efficient acylation and diverse synthetic applications, showcasing its versatility in organic chemistry. | ||||||
Ethyl (2-bromobenzoyl)acetate | 50671-05-1 | sc-227999 | 1 g | $111.00 | ||
Ethyl (2-bromobenzoyl)acetate is a distinctive carbonyl compound characterized by its electrophilic nature, primarily due to the presence of the bromine atom, which enhances its reactivity in nucleophilic acyl substitution reactions. The compound exhibits unique steric effects that influence reaction pathways, leading to selective formation of products. Its ability to engage in intramolecular interactions can also affect the stability of intermediates, thereby impacting overall reaction kinetics and efficiency. | ||||||
DIF-3 | 113411-17-9 | sc-257347 | 1 mg | $136.00 | ||
DIF-3, as a carbonyl compound, showcases remarkable reactivity due to its acid halide characteristics. The presence of the carbonyl group enables rapid acyl transfer reactions, making it a potent electrophile. Its unique steric environment promotes selective interactions with nucleophiles, leading to distinct reaction pathways. Additionally, the compound's ability to form stable intermediates enhances its utility in various synthetic transformations, highlighting its dynamic role in organic synthesis. | ||||||
4′-Chloro-5-fluoro-2-hydroxybenzophenone | 62433-26-5 | sc-233106 | 5 g | $300.00 | ||
4'-Chloro-5-fluoro-2-hydroxybenzophenone is a notable carbonyl compound distinguished by its dual halogen substituents, which significantly modulate its electronic properties and reactivity. The presence of the hydroxyl group introduces hydrogen bonding capabilities, enhancing solubility in polar solvents. This compound exhibits unique photophysical behavior, with potential for strong UV absorption, influencing its interactions in photochemical processes and affecting reaction dynamics in various environments. | ||||||
Methyl 4-(3-hydroxyphenyl)benzoate | 579511-01-6 | sc-235752 | 5 g | $528.00 | ||
Methyl 4-(3-hydroxyphenyl)benzoate is a carbonyl compound characterized by its ester functionality, which facilitates nucleophilic attack in various organic reactions. The hydroxyl group enhances its ability to engage in intramolecular hydrogen bonding, influencing its conformational stability. This compound exhibits notable dipole moments due to its polar functional groups, affecting its solubility and reactivity in different solvents, and potentially altering reaction kinetics in synthetic pathways. | ||||||
3-Ethoxy-4-hydroxybenzaldehyde | 121-32-4 | sc-238538 | 100 g | $31.00 | ||
3-Ethoxy-4-hydroxybenzaldehyde, a notable carbonyl compound, features an ethoxy group that enhances its solubility in organic solvents, promoting diverse reactivity. The hydroxy group can participate in intramolecular hydrogen bonding, stabilizing transition states during reactions. Its carbonyl carbon is susceptible to nucleophilic addition, while the aromatic ring can undergo electrophilic substitution, allowing for tailored modifications. This compound's unique structural attributes enable it to serve as a key building block in synthetic chemistry. | ||||||
Benactyzine hydrochloride | 57-37-4 | sc-233927 | 10 g | $42.00 | 1 | |
Benactyzine hydrochloride is a carbonyl compound characterized by its unique structural features that influence its reactivity. The presence of a carbonyl group enhances its electrophilic nature, allowing for significant interactions with nucleophiles. Its molecular geometry contributes to specific steric hindrances, which can modify reaction kinetics and pathways. Additionally, the compound exhibits notable solubility in various solvents, driven by its polar characteristics and intermolecular forces. | ||||||