Acid Halides
Items 11 to 20 of 374 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-Bromothiophene-3-carbonyl chloride | 72899-51-5 | sc-261865 sc-261865A | 250 mg 1 g | $129.00 $216.00 | ||
4-Bromothiophene-3-carbonyl chloride is a potent acid halide characterized by its unique thiophene ring structure, which imparts distinct electronic properties. The presence of the bromine atom enhances its electrophilicity, promoting rapid nucleophilic attack. This compound exhibits a high degree of reactivity, particularly in acylation reactions, where it can form stable intermediates. Its moderate boiling point and solubility in organic solvents facilitate efficient handling in synthetic processes, making it a versatile reagent in organic chemistry. | ||||||
Acetyl chloride | 75-36-5 | sc-207253 sc-207253A | 25 g 500 g | $30.00 $50.00 | ||
Acetyl chloride is a highly reactive acid halide known for its ability to undergo nucleophilic acyl substitution reactions. Its carbonyl carbon is electrophilic, making it susceptible to attack by nucleophiles, leading to the formation of acyl derivatives. The presence of the chlorine atom enhances its reactivity, facilitating rapid esterification and acylation processes. Additionally, it can participate in Friedel-Crafts acylation, showcasing its versatility in organic synthesis. | ||||||
Butyryl chloride | 141-75-3 | sc-239451 | 250 g | $34.00 | ||
Butyryl chloride is a versatile acid halide known for its strong electrophilic nature, primarily due to the presence of a carbonyl group adjacent to a halogen. This configuration promotes rapid nucleophilic attack, leading to the formation of various acyl derivatives. It is a colorless liquid with a distinctive, sharp odor and a relatively low boiling point. The compound's reactivity is further modulated by its chain length, influencing reaction kinetics and selectivity in synthetic pathways. | ||||||
Hexanoyl chloride | 142-61-0 | sc-250109 sc-250109A | 25 ml 100 ml | $45.00 $67.00 | ||
Hexanoyl chloride is a potent acid halide characterized by its strong electrophilic carbonyl group, which readily engages in nucleophilic attacks. The chlorine atom significantly increases its reactivity, allowing for swift acylation reactions. This compound can also promote the formation of anhydrides and esters through its interactions with alcohols and amines. | ||||||
Nonafluoropentanoyl chloride | 375-60-0 | sc-263959 | 5 g | $270.00 | ||
Nonafluoropentanoyl chloride is a highly reactive acid halide distinguished by its perfluorinated carbon chain, which imparts unique electronic properties. The presence of fluorine atoms enhances the electrophilicity of the carbonyl carbon, facilitating rapid acylation with nucleophiles. This compound exhibits remarkable stability against hydrolysis, allowing for controlled reactions in diverse environments. Its distinct molecular interactions enable the formation of complex derivatives, expanding its utility in synthetic chemistry. | ||||||
5H-Octafluorovaleroyl chloride | 376-71-6 | sc-262740 | 1 g | $74.00 | ||
5H-Octafluorovaleroyl chloride is an acid halide characterized by its unique fluorinated structure, which enhances its electrophilicity. This compound readily participates in acylation reactions, forming stable acyl derivatives with nucleophiles. Its strong electron-withdrawing fluorine atoms influence reaction kinetics, promoting rapid esterification and amidation processes. | ||||||
2-Chlorobenzoyl chloride | 609-65-4 | sc-237995 | 100 g | $29.00 | ||
2-Chlorobenzoyl chloride is a reactive acid halide known for its ability to engage in acylation reactions with various nucleophiles, leading to the formation of diverse acyl derivatives. The presence of the chlorine atom enhances its electrophilic nature, facilitating rapid reaction kinetics. This compound exhibits unique solubility properties due to its aromatic structure, influencing its interactions in organic synthesis and making it a key player in the development of complex molecular architectures. | ||||||
Methyl 4-chloro-4-oxobutyrate | 1490-25-1 | sc-250357 sc-250357A | 5 g 25 g | $37.00 $106.00 | ||
Methyl 4-chloro-4-oxobutyrate is a versatile acid halide characterized by its electrophilic carbonyl group, which readily participates in nucleophilic acyl substitution reactions. The presence of the chloro substituent enhances its reactivity, allowing for efficient formation of esters and amides. Its unique steric and electronic properties facilitate selective reactions, making it an important intermediate in synthetic pathways. Additionally, its polar nature influences solubility and reactivity in various organic solvents. | ||||||
Bromodifluoroacetyl bromide | 1796-12-9 | sc-263057 sc-263057A | 10 g 25 g | $497.00 $940.00 | ||
Bromodifluoroacetyl bromide is a reactive acid halide distinguished by its dual bromine substituents and electron-withdrawing fluorine atoms. This configuration enhances its electrophilicity, promoting rapid nucleophilic attack. The compound's unique steric hindrance and polar characteristics lead to selective reactivity in acylation reactions, facilitating the formation of diverse carbonyl derivatives. Its strong dipole moment also influences solvation dynamics, impacting reaction kinetics in various environments. | ||||||
α-Chlorophenylacetyl chloride | 2912-62-1 | sc-239154 | 10 g | $286.00 | ||
α-Chlorophenylacetyl chloride is a potent acid halide characterized by its chlorinated aromatic structure, which significantly enhances its electrophilic nature. The presence of the chlorine atom increases the compound's reactivity towards nucleophiles, facilitating acylation processes. Its unique steric profile allows for selective interactions with various nucleophiles, leading to distinct reaction pathways. Additionally, the compound's polar characteristics influence solubility and reactivity in diverse solvents, affecting overall reaction rates. | ||||||