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161462-35-7

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161462-35-7 Usage

Class

Cyclopropylketones

Contains

Cyclopropyl group
Trifluoromethyl group
Methylsulfanyl group

Physical appearance

Yellow to brown powder

Molecular weight

350.36 g/mol

Applications

Organic synthesis
Pharmaceutical research

Potential

Biological activity
Therapeutic applications

Safety precautions

Handle with caution and follow proper safety protocols due to potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 161462-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,4,6 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 161462-35:
(8*1)+(7*6)+(6*1)+(5*4)+(4*6)+(3*2)+(2*3)+(1*5)=117
117 % 10 = 7
So 161462-35-7 is a valid CAS Registry Number.

161462-35-7Downstream Products

161462-35-7Relevant articles and documents

Preparation method of isoxaflutole key intermediate

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Paragraph 0028; 0032-0033; 0035-0036; 0038-0039; 0041, (2021/06/23)

The invention relates to the field of pesticide chemistry, in particular to a preparation method of an isoxaflutole key intermediate. The preparation method comprises the steps of under the protection of inert gas, dissolving 1-(2-(methylthio)-4-(trifluoromethyl) phenyl) ethanone and cyclopropane formonitrile in an organic solvent, adding strong base, carrying out heat treatment reaction on the mixture, adding acidizing fluid to adjust the pH value to be neutral after the reaction is completed, separating out a water phase, and concentrating an organic phase to obtain an intermediate I; and dissolving the intermediate I in an organic solvent, adding water and strong acid, carrying out a heat treatment reaction, separating a water phase after the reaction is completed, and concentrating an organic phase to obtain the 1-cyclopropyl-3-(2-(methylthio)-4-(trifluoromethyl) phenyl) propyl-1, 3-diketone. The preparation method of the isoxaflutole key intermediate provided by the invention has the advantages of mild reaction, less generation of impurities and solid wastes, improvement of the yield and purity of the product, and reduction of the production cost, and is suitable for industrial production.

Preparation method of 1-cyclopropyl-3-(2-methylthio-4-trifluoromethylphenyl)propyl-1,3-dione

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Paragraph 0052; 0059-0061, (2019/07/04)

The invention provides a preparation method of 1-cyclopropyl-3-(2-methylthio-4-trifluoromethylphenyl)propyl-1,3-dione, and belongs to the technical field of organic synthesis. The preparation method comprises following steps: (1) mixing 2-nitro-4-trifluor

Preparation of C1-C5 alkyl esters of nitro or thioether substituted aromatic carboxylic acids

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Example 11, (2010/11/29)

Methods for preparing substituted aromatic carboxylic acid esters are described. In particular, the invention relates a method for preparing a nitro-substituted aromatic carboxylic acid ester: Additionally the invention relates to a method for preparing a

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