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4-chloro-α-(4-chlorophenyl)-α-(pentafluoroethyl)-benzenemethanol is a complex organic compound with the molecular formula C14H8Cl2F5O. It is characterized by a benzene ring with a 4-chloro substituent, an α-(4-chlorophenyl) group, and an α-(pentafluoroethyl) group attached to the benzene ring. The molecule also contains a methanol functional group, which is a hydroxyl group (-OH) attached to a methyl group (-CH3). 4-chloro-α-(4-chlorophenyl)-α-(pentafluoroethyl)-benzenemethanol is likely to be used in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and potential reactivity. Its properties, such as solubility, stability, and reactivity, would be influenced by the presence of the halogenated and fluorinated substituents, making it a potentially interesting candidate for further chemical research and development.

357-51-7

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357-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 357-51-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 357-51:
(5*3)+(4*5)+(3*7)+(2*5)+(1*1)=67
67 % 10 = 7
So 357-51-7 is a valid CAS Registry Number.

357-51-7Relevant academic research and scientific papers

Nucleophilic perfluoroalkylation of imines and carbonyls: Perfluoroalkyl sulfones as efficient perfluoroalkyl-transfer motifs

Prakash, G. K. Surya,Wang, Ying,Mogi, Ryo,Hu, Jinbo,Mathew, Thomas,Olah, George A.

supporting information; experimental part, p. 2932 - 2935 (2010/09/09)

Alkoxide-induced nucleophilic pentafluoroethylation and trifluoromethylation of aldehydes, ketones, and imines using pentafluoroethyl phenyl sulfone (PhSO2CF2CF3, 1) and trifluoromethyl phenyl sulfone (PhSO2CF3, 2), respectively, have been successfully achieved. High diastereoselectivity was observed during the perfluoroalkylation of homochiral sulfinimines to give the corresponding perfluoroalkyl sulfinamides.

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