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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.
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Oxydiethylene bis(chloroformate) CAS:106-75-2
Oxydiethylene bis(chloroformate) is a symmetrical organic compound featuring two chloroformate functional groups attached to an oxydiethylene backbone. This diacyl chloride serves as a potent acylating agent in organic synthesis, facilitating the formation of carbamates and esters through nucleophilic substitution reactions with amines and alcohols. Its unique structure enhances its reactivity, making it invaluable in the fields of pharmaceuticals, agrochemicals, and polymer chemistry. The versatility of oxydiethylene bis(chloroformate) allows for the modification of various nucleophiles, resulting in diverse chemical products. Understanding its properties and handling precautions is essential for chemists utilizing this important reagent in synthetic processes.
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4-Methylvaleryl chloride CAS:38136-29-7
4-Methylvaleryl chloride, also known as 4-methylpentanoyl chloride, is an organic compound categorized as an acyl chloride. Derived from 4-methylvaleric acid, it features a five-carbon backbone with a methyl group at the fourth position and a highly reactive acyl chloride functional group. This compound is primarily used in organic synthesis as an acylating agent, facilitating nucleophilic substitution reactions with alcohols and amines to form esters and amides. Its unique structure and reactivity make 4-methylvaleryl chloride a valuable intermediate in the synthesis of various chemical compounds, particularly in pharmaceutical and agrochemical applications.
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DIALLYLCARBAMYL CHLORIDE CAS:25761-72-2
Diallylcarbamyl chloride is an organic compound belonging to the class of carbamates and acyl chlorides. Featuring a central carbon atom bonded to two allyl groups and a carbamyl chloride functional group, this compound exhibits significant reactivity and versatility in organic synthesis. Diallylcarbamyl chloride serves as an effective acylating agent, facilitating nucleophilic substitution reactions with amines and alcohols to form various derivatives, including amides and esters. Its unique structure also makes it useful in the development of pharmaceuticals, agrochemicals, and polymeric materials, where its functional groups can be exploited for specific chemical transformations.
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Acetoxyacetyl chloride CAS:13831-31-7
Acetoxyacetyl chloride is an organic compound classified as an acyl chloride, derived from the reaction of acetic anhydride and acetyl chloride. It features both acetoxy and acyl chloride functional groups, making it a versatile reagent in organic synthesis. This compound serves primarily as an acylating agent, facilitating the formation of various derivatives, including esters and amides, through nucleophilic substitution reactions with alcohols and amines. Acetoxyacetyl chloride’s unique structure imparts specific chemical properties that are beneficial in pharmaceutical and agrochemical applications, enabling chemists to create a diverse array of compounds efficiently.
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1,4-Phenylene diisocyanate CAS:104-49-4
1,4-Phenylene diisocyanate (PDI), also known as 1,4-benzenediamine diisocyanate, is an aromatic compound characterized by the presence of two isocyanate (-N=C=O) functional groups attached to a phenylene ring. This compound is primarily utilized in the production of polyurethanes and other polymers due to its reactivity and ability to cross-link with various polyols. Its unique structure allows for the synthesis of rigid and flexible foams, elastomers, and coatings with enhanced mechanical properties and chemical resistance. Additionally, PDI plays a significant role in the development of specialty materials in industries such as automotive, construction, and textiles.
