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2,3,4,5-Tetrachlorobenzoyl chloride is a chemical compound characterized by the molecular formula C7HCl4O. It is a colorless to pale yellow liquid known for its versatility as an intermediate in the synthesis of various products, including pharmaceuticals, agricultural chemicals, and dyes. 2,3,4,5-Tetrachlorobenzoyl chloride is recognized for its reactivity, enabling the formation of strong covalent bonds with a range of organic and inorganic compounds, and for its potency as an acylating agent, capable of transferring its acyl group to other compounds in chemical synthesis processes.

42221-52-3

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42221-52-3 Usage

Uses

Used in Pharmaceutical Industry:
2,3,4,5-Tetrachlorobenzoyl chloride is used as a synthetic intermediate for the development of pharmaceuticals, leveraging its reactivity to form essential covalent bonds in the creation of new drug molecules.
Used in Agricultural Chemicals:
In the agricultural sector, 2,3,4,5-Tetrachlorobenzoyl chloride is utilized as a key component in the production of fungicides and herbicides, contributing to the development of effective crop protection agents.
Used in Dye Industry:
2,3,4,5-Tetrachlorobenzoyl chloride serves as an intermediate in the synthesis of dyes, where its acylating properties are employed to produce a variety of colorants for different applications.
Used in Organic Synthesis:
2,3,4,5-Tetrachlorobenzoyl chloride is used as a reagent in organic synthesis, taking advantage of its ability to form strong covalent bonds, which is crucial for the construction of complex organic molecules.
However, due to its high toxicity and corrosive nature, 2,3,4,5-Tetrachlorobenzoyl chloride requires meticulous handling and storage to ensure the safety of human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 42221-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,2 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42221-52:
(7*4)+(6*2)+(5*2)+(4*2)+(3*1)+(2*5)+(1*2)=73
73 % 10 = 3
So 42221-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C7HCl5O/c8-3-1-2(7(12)13)4(9)6(11)5(3)10/h1H

42221-52-3Relevant academic research and scientific papers

Preparation method of benzoyl chloride compound

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Paragraph 0069-0073, (2021/06/22)

The invention provides a preparation method of a benzoyl chloride compound. The preparation method comprises the following step: with a trichloromethyl benzene compound and a benzoic acid compound as raw materials and ferric oxide as a catalyst, carrying out a catalytic reaction to prepare the benzoyl chloride compound. According to the method disclosed by the invention, the benzoyl chloride compound can be obtained under the condition of not using a solvent, yield is up to 95% or above, atom economy is good, cost is lower, operation is simpler, more convenient and safer, the treatment amount of three wastes is smaller, the three wastes is easier to treat, and the method is more suitable for industrial production.

Tetrachloro benzoyl chloride synthesis method (by machine translation)

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Paragraph 0016; 0017; 0019, (2018/03/25)

The invention relates to a synthesis method of tetrachloro benzoyl chloride, the specific step includes: A. at the end face of proper amount added in tetrachloro phthalic anhydride, potassium carbonate and distilled water stirring and heating, temperature

Preparation method of 2,3,4,5-tetrachlorobenzoyl chloride

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Paragraph 0016; 0017; 0019, (2018/03/25)

The invention relates to a preparation method of 2,3,4,5-tetrachlorobenzoyl chloride. The preparation method comprises the specific steps: A, adding a proper amount of tetrachlorophthalic anhydride, sodium hydroxide and distilled water into a pressure ket

High-yield 2,3,4,5-tetrachlorobenzoyl chloride preparation method

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Paragraph 0012-0015, (2018/04/01)

The invention discloses a high-yield 2,3,4,5-tetrachlorobenzoyl chloride preparation method. 2,3,4,5-tetrachlorobenzoic acid is firstly prepared from tetrachlorophthalic anhydride used as a raw material, then the final product 2,3,4,5-tetrachlorobenzoyl c

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