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α-(2,2,2-trifluoro-1-phenylethoxy) propanoic acid is a complex organic compound with the molecular formula C11H9F3O3. It is characterized by the presence of a trifluoro-phenylethoxy group attached to a propanoic acid backbone. This chemical is known for its unique properties, such as its ability to form hydrogen bonds due to the carboxylic acid group, and its increased lipophilicity and reactivity due to the presence of fluorine atoms. It is often used in the synthesis of pharmaceuticals and agrochemicals, where its specific structural features can enhance the activity or selectivity of the final product. The compound's stability and reactivity make it a valuable intermediate in the development of new drugs and chemical compounds.

70782-58-0

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70782-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70782-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,8 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70782-58:
(7*7)+(6*0)+(5*7)+(4*8)+(3*2)+(2*5)+(1*8)=140
140 % 10 = 0
So 70782-58-0 is a valid CAS Registry Number.

70782-58-0Downstream Products

70782-58-0Relevant academic research and scientific papers

Derivatives of arylalkanoic acids, compositions and use

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, (2008/06/13)

There are now described some novel alpha-[1-aryl-2,2,2-trifluoroethoxy (or-ethylthio)]alkanoic acids that are useful for reducing triglycerides and cholesterol levels in the blood of animals. The percentage reduction in test rats has been observed to be from 20 to 65 for triglycerides and from 15 to 50 for cholesterol. A representative compound of the invention is alpha-(2,2,2-trifluoro-1-phenyl-1-ethoxy)butyric acid. Most of the compounds have an LD50 greater than 800 mg/kg, intraperitoneally, in male mice. A method of use, compositions, and a process for synthesis are also described.

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