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2,2,2-Trichloro-1-(2,4-dimethoxy-phenyl)-ethanone is a chemical compound characterized by the presence of three chlorine atoms and a 2,4-dimethoxyphenyl ring attached to an ethanone group. 2,2,2-trichloro-1-(2,4-dimethoxy-phenyl)-ethanone serves as a versatile building block in organic chemistry, playing a crucial role in the synthesis of a wide range of pharmaceuticals, agrochemicals, fragrances, dyes, and flavoring agents.

76569-41-0

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76569-41-0 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2,2,2-Trichloro-1-(2,4-dimethoxy-phenyl)-ethanone is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new molecules with potential therapeutic and pesticidal properties, contributing to advancements in medicine and agriculture.
Used in Fragrance Industry:
In the fragrance industry, 2,2,2-trichloro-1-(2,4-dimethoxy-phenyl)-ethanone is utilized as a precursor for the production of various scent compounds. Its ability to form a wide array of aromatic molecules makes it a valuable component in creating unique and complex fragrances.
Used in Dye Industry:
2,2,2-Trichloro-1-(2,4-dimethoxy-phenyl)-ethanone is employed as a building block in the synthesis of dyes for various applications, including textiles, plastics, and printing inks. Its versatility in forming colored compounds contributes to the development of new and innovative dyes with improved properties.
Used in Flavoring Agent Industry:
2,2,2-trichloro-1-(2,4-dimethoxy-phenyl)-ethanone is also used in the production of flavoring agents for the food and beverage industry. Its ability to form a variety of taste compounds allows for the creation of unique and appealing flavors, enhancing the sensory experience of various products.
Safety Precautions:
Due to its toxic, corrosive nature, and potential to cause irritation to the skin, eyes, and respiratory system, 2,2,2-trichloro-1-(2,4-dimethoxy-phenyl)-ethanone should be handled with extreme caution. It is essential that only trained professionals work with 2,2,2-trichloro-1-(2,4-dimethoxy-phenyl)-ethanone in a controlled laboratory environment, following strict safety protocols to minimize risks and ensure the well-being of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 76569-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,6 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76569-41:
(7*7)+(6*6)+(5*5)+(4*6)+(3*9)+(2*4)+(1*1)=170
170 % 10 = 0
So 76569-41-0 is a valid CAS Registry Number.

76569-41-0Downstream Products

76569-41-0Relevant academic research and scientific papers

The Chemistry of Nitrilium Salts. Part 1. Acylation of Phenols and Phenol Ethers with Nitriles and Trifluoromethanesulphonic Acid

Booth, Brian L.,Noori, Ghazi F.M.

, p. 2894 - 2900 (2007/10/02)

Aliphatic nitriles, RCN (R = Me, n-Pr, CH2Cl, and CCl3), in the presence of trifluoromethanesulphonic acid have been found to react with a number of mono-, di-, and tri-substituted phenols and phenol ethers at room temperature to give ketones after hydrolysis of the reaction mixture.Moderate to good yields of acylation products are obtained in the majority of these reactions.The yield with malononitrile and succinonitrile, which are only slightly soluble in the reaction medium, are generally poor, and reaction involves only one of the available nitrile groups.Attempts to use diethyl ether and dichloromethane as solvents for some of these reactions were unsuccessful, but limited success was achieved with nitromethane.

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