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Acylation reaction under the action of acyl chloride

Acylation reaction under the action of acyl chloride

Acyl chloride, whose English name is Acyl chloride, is a highly chemically reactive acylation reagent. It is a general term for a class of organic compounds, possessing strong hygroscopicity and deliquescence, and capable of undergoing vigorous hydrolysis reactions with water.

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Acid chloride

Acid chloride

Acid chlorides are important carboxylic acid derivatives with significant applications in organic synthesis and pharmaceutical synthesis. They can undergo various reactions, including hydrolysis, alcoholysis, ammonolysis (aminolysis), reactions with organometallic reagents, reduction reactions, and α-hydrogen halogenation.

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[Chemical Engineering Knowledge]: Preparation and Precautions of Acid Chlorides

[Chemical Engineering Knowledge]: Preparation and Precautions of Acid Chlorides

In chemical laboratories, acyl chlorides are commonly used compounds with a wide range of applications. However, during the preparation and use of acyl chlorides, certain precautions must be taken to ensure operational safety and the smooth progress of experiments.

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[Forward] The most comprehensive ever! Exploring the properties, preparation, monitoring, post-processing, and subsequent reactions of acyl chlorides in one article

[Forward] The most comprehensive ever! Exploring the properties, preparation, monitoring, post-processing, and subsequent reactions of acyl chlorides in one article

Acid halides are derivatives obtained by replacing the hydroxyl group in carboxylic acids with halogens (fluorine, chlorine, bromine, iodine). Acid halides are very reactive compounds that do not exist in nature and can only be obtained through chemical synthesis.

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Physicochemical properties and pharmaceutical applications of n-butyryl chloride

Physicochemical properties and pharmaceutical applications of n-butyryl chloride

Butyryl chloride, with the English name Butyryl chloride, is a transparent yellowish liquid at room temperature and pressure, has strong hygroscopicity and is relatively sensitive to water, and is soluble in common organic solvents including ethyl acetate and dichloromethane. Butyryl chloride belongs to the alkyl acyl chloride compounds, possesses extremely high chemical reactivity, and can undergo acylation reactions with common alcohols or amine compounds, widely applied in the structural modification and synthesis of pesticide molecules.

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Synthesis and Applications of Valeryl Chloride

Synthesis and Applications of Valeryl Chloride

Valeryl chloride (also known as n-pentanoyl chloride or n-valeryl chloride) is a colorless, transparent, fuming oily liquid with an irritating odor. Its chemical formula is C₅H₉ClO, and its structural formula is CH₃CH₂CH₂CH₂COCl. It decomposes on contact with water.

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Preparation and application of capryloyl chloride

Preparation and application of capryloyl chloride

Octanoyl chloride is a colorless, transparent liquid at room temperature and pressure. It has a pungent odor and is soluble in most organic solvents, but it is easily deliquesced when exposed to water.

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Emergency Response Plan for Acyl Chloride

Emergency Response Plan for Acyl Chloride

Acyl chloride (acid chloride) is a common organic compound, widely used in industries such as medicine, pesticides, dyes, plastics, and coatings. Acyl chloride has active chemical properties, reacts vigorously with substances like water, alcohols, and amines, producing a strong irritating odor, and is flammable and explosive.

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