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Ethyl lauroyl arginate hydrochloride CAS:60372-77-2
Ethyl lauroyl arginate hydrochloride is a multifunctional compound derived from the amino acid arginine and lauric acid. This cationic surfactant is known for its antimicrobial properties, making it a valuable ingredient in personal care products, food preservation, and pharmaceuticals. Its ability to enhance product stability and efficacy while offering conditioning benefits makes it suitable for formulations such as shampoos, conditioners, and skin care products. Additionally, its safety profile and biodegradability contribute to its appeal in developing sustainable and effective cosmetic and health-related applications.
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Bis(5-oxo-L-prolinato-N1,O2)zinc CAS: 15454-75-8
Bis(5-oxo-L-prolinato-N1,O2)zinc is a coordination compound formed from zinc and 5-oxo-L-proline, an amino acid derivative. This complex showcases unique properties due to the chelating nature of the proline-derived ligand, resulting in enhanced stability and solubility compared to uncoordinated forms. Its applications span various fields, including biochemistry, pharmacology, and materials science, where it serves as a potential therapeutic agent, catalyst, or stabilizer. Understanding its chemical structure and reactivity is essential for leveraging its capabilities in innovative applications.
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4-Nitrobenzyl chloroformate CAS:4457-32-3
4-Nitrobenzyl chloroformate is an important organic compound widely used in synthetic chemistry. This reagent features a 4-nitrobenzyl group attached to a chloroformate moiety, making it valuable for various chemical transformations. The presence of the nitro group enhances the electrophilicity of the carbonyl carbon, facilitating its reactivity with nucleophiles. It finds applications in synthesizing esters, carbonates, and other derivatives, playing a significant role in pharmaceutical and agrochemical development. Understanding its properties and reactions is vital for chemists seeking to leverage this compound in creating complex organic molecules.
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4-CHLOROPHENYL CHLOROFORMATE CAS:7693-45-0
4-Chlorophenyl chloroformate is an important organic compound utilized in various synthetic chemistry applications. This compound contains a 4-chlorophenyl group linked to a chloroformate functional group, making it a valuable reagent for acylation reactions. The presence of the chlorine atom increases the electrophilicity of the carbonyl carbon, facilitating nucleophilic attacks by alcohols and amines. Due to its reactivity, 4-chlorophenyl chloroformate finds extensive use in pharmaceutical synthesis, agrochemical development, and the production of complex organic molecules. Understanding its properties and behaviors is essential for chemists aiming to effectively utilize this versatile compound in their research.
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Neodecanoyl chloride CAS:40292-82-8
Neodecanoyl chloride is an acyl chloride derived from neodecanoic acid, characterized by its long hydrocarbon chain and a carbonyl group attached to a chlorine atom. This compound serves as a powerful acylating agent in organic synthesis, facilitating the formation of esters, amides, and other carbonyl-containing compounds through nucleophilic substitution reactions. Given its reactivity, neodecanoyl chloride is widely utilized in the fields of pharmaceuticals, agrochemicals, and polymer chemistry. Its unique structure enables it to impart specific properties to the resulting compounds, making it an essential reagent for chemists aiming to develop complex organic molecules.
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3-Methoxybutyl chloroformate CAS:75032-87-0
3-Methoxybutyl chloroformate is an organic compound that features a chloroformate functional group attached to a 3-methoxybutyl group. As a versatile acylating agent, it plays a significant role in organic synthesis, facilitating the formation of esters and carbamates through nucleophilic substitution reactions with alcohols and amines. The presence of the methoxy group enhances the electrophilicity of the carbonyl carbon, improving its reactivity. This compound finds applications in pharmaceuticals, agrochemicals, and polymer chemistry, where it aids in the synthesis of biologically active molecules. Understanding its properties and reactivity is essential for chemists working with this important reagent.
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4-BROMOPHENYL CHLOROFORMATE CAS:7693-44-9
4-Bromophenyl chloroformate is a significant chemical compound used in organic synthesis, characterized by the presence of a brominated phenyl group attached to a chloroformate moiety. This compound acts as a versatile acylating agent, facilitating various chemical reactions that lead to the formation of esters and carbamates. The bromine atom enhances the electrophilic characteristics of the chloroformate carbon, allowing for efficient nucleophilic attacks by alcohols and amines. Its applications extend into the pharmaceutical and agrochemical sectors, where it contributes to the development of biologically active compounds. Understanding its reactivity is crucial for chemists aiming to utilize this reagent effectively.
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2-Phenoxyethyl chloroformate CAS:34743-87-8
2-Phenoxyethyl chloroformate is a notable organic compound characterized by the presence of a phenoxy group attached to a chloroformate functional group. This reagent serves primarily as an acylating agent in organic synthesis, facilitating the formation of esters and carbamates through nucleophilic substitution reactions with alcohols and amines. The phenoxyethyl moiety imparts unique properties that can modify the solubility and reactivity of target compounds. Its applications are widespread in pharmaceutical development, agrochemicals, and materials science, making it an essential tool for chemists looking to create complex organic structures. Understanding its reactivity is crucial for effective utilization in synthetic pathways.
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2-Ethoxyethyl chloroformate CAS:628-64-8
2-Ethoxyethyl chloroformate is an organic compound comprising a chloroformate functional group attached to a 2-ethoxyethyl moiety. This reagent functions as a powerful acylating agent in organic synthesis, facilitating the formation of esters and carbamates through reactions with nucleophiles such as alcohols and amines. The ethoxy substituent enhances the solubility and reactivity of the resultant compounds, making them suitable for various applications in pharmaceuticals, agrochemicals, and polymer chemistry. Understanding the properties and reactivity of 2-ethoxyethyl chloroformate is essential for chemists aiming to utilize this compound effectively in diverse synthetic strategies.
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3-Chloropropyl chloroformate CAS:628-11-5
3-Chloropropyl chloroformate is a specialized organic compound widely utilized in synthetic chemistry. It features a chloropropyl group linked to a chloroformate functional group, making it an important reagent in the production of esters, carbonates, and other derivatives. The presence of chlorine atoms enhances its reactivity, allowing it to participate in various nucleophilic substitution reactions. Its applications extend beyond just synthesis; it serves as a building block in pharmaceutical development, agrochemical formulations, and polymer chemistry. Understanding its properties and reactivity is essential for chemists aiming to harness this compound effectively in diverse chemical processes.
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Lauryl chloroformate CAS:24460-74-0
Lauryl chloroformate is an important organic compound featuring a long-chain lauryl group attached to a chloroformate functional group. This compound serves as a versatile acylating agent in organic synthesis, particularly in the formation of esters and carbonates. The lauryl moiety, derived from lauric acid, imparts hydrophobic characteristics, making it beneficial for modifying the solubility and lipophilicity of target compounds. Lauryl chloroformate finds applications in pharmaceutical development, agrochemicals, and polymer chemistry. A thorough understanding of its reactivity and properties is essential for chemists aiming to leverage this compound effectively in various synthetic pathways.
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4-METHOXYPHENYL CHLOROFORMATE CAS:7693-41-6
4-Methoxyphenyl chloroformate is an organic compound featuring a 4-methoxy substituted aromatic ring linked to a chloroformate functional group. This compound functions as a versatile acylating agent in organic synthesis, facilitating the formation of esters and carbamates by reacting with nucleophiles such as alcohols and amines. The methoxy substituent enhances the electrophilic character of the chloroformate carbon, improving reactivity during acylation reactions. Its applications span across pharmaceutical development, agrochemicals, and materials science, where it contributes to the synthesis of biologically active compounds. Understanding its properties and reactivity patterns is essential for chemists using this compound effectively.
