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4-Chloro-4'-(chlorodifluoromethoxy)benzophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

279684-18-3

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279684-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 279684-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,6,8 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 279684-18:
(8*2)+(7*7)+(6*9)+(5*6)+(4*8)+(3*4)+(2*1)+(1*8)=203
203 % 10 = 3
So 279684-18-3 is a valid CAS Registry Number.

279684-18-3Downstream Products

279684-18-3Relevant academic research and scientific papers

Short synthesis of 4-chloro-4′-(chlorodifluoromethoxy)benzophenone

Karrer, Friedrich,Meier, Hans,Pascual, Alfons

, p. 81 - 84 (2000)

A one-pot, highly selective synthesis of 4-chloro-4′-(chlorodifluoromethoxy)benzophenone suitable for an industrial scale-up was developed. Fluorination of 4-(trichloromethoxy)benzoyl chloride at -20°C with HF to 4-(chlorodifluoromethoxy)benzoyl fluoride followed by an in situ Friedel-Crafts reaction with chlorobenzene in the presence of BF3 at -5°C yielded the title compound in excellent yield.

Synthesis and structure-activity relationships of benzophenone hydrazone derivatives with insecticidal activity

Boeger, Manfred,Duerr, Dieter,Gsell, Laurenz,Hall, Roger G.,Karrer, Friedrich,Kristiansen, Odd,Maienfisch, Peter,Pascual, Alfons,Rindlisbacher, Alfred

, p. 191 - 202 (2007/10/03)

A broad range of benzophenone hydrazone derivatives was prepared and tested against selected chewing insect pests, allowing the analysis of structure-activity relationships. Good activity was found only when the aromatic rings were substituted at the 4-positions with an halogen atom and a triflate or perhaloalkoxy group. In contrast, a number of substituents on the hydrazone part led to active compounds, the best results being achieved with acyl-type substituents. The excellent laboratory and greenhouse activity of the best representatives was confirmed in semi-field trials against Spodoptera littoralis. ° 2001 Society of Chemical Industry.

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