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Benzenemethanol, 3,5-dichloro-α-phenyl-α-(trifluoromethyl)-, 4-methylbenzenesulfonate is a complex organic chemical compound with the molecular formula C15H12Cl2F3O3S. It is a derivative of benzenemethanol, featuring a 3,5-dichloro substitution on the benzene ring, an α-phenyl-α-(trifluoromethyl) group, and a 4-methylbenzenesulfonate ester functional group. Benzenemethanol, 3,5-dichloro-a-phenyl-a-(trifluoromethyl)-, 4-methylbenzenesulfonate is characterized by its unique structure, which includes a combination of chlorine, fluorine, and sulfur atoms, as well as a methyl group on the benzene ring. It is likely to be used in the synthesis of pharmaceuticals or other specialty chemicals due to its diverse functional groups, which can participate in various chemical reactions. The compound's specific applications and properties would depend on its reactivity and stability, which are influenced by the presence of these functional groups.

96236-00-9

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96236-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96236-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,3 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96236-00:
(7*9)+(6*6)+(5*2)+(4*3)+(3*6)+(2*0)+(1*0)=139
139 % 10 = 9
So 96236-00-9 is a valid CAS Registry Number.

96236-00-9Downstream Products

96236-00-9Relevant academic research and scientific papers

Substituent Effects on the Solvolysis of 1,1-Diphenyl-2,2,2-trifluoroethyl Tosylates: Comparison between Symmetrically Disubstituted and Monosubstituted Systems

Fujio, Mizue,Morimoto, Hiroshi,Kim, Hyun-Joong,Tsuno, Yuho

, p. 1403 - 1411 (2007/10/03)

The solvolysis rates of 1-(substituted phenyl)-1-phenyl-2,2,2-trifluoroethyl and 1,1-bis(substituted phenyl)-2,2,2-trifluoroethyl tosylates or bromides were conductimetrically measured at 25.0 °C in 80% aqueous ethanol. The substituent effects on these so

SOLVOLYTIC STUDIES OF THE HIGHLY CROWDED 1-ARYL-1-PHENYL-1-(TRIFLUOROMETHYL)METHYL BR0MIDE AND TOSYLATES

Liu, Kwang-Ting,Kuo, Mann-Yan

, p. 355 - 358 (2007/10/02)

In the titled system the remarkably high tosylate/bromide solvolysis rate ratio of 1.56E6:1 indicates a highly strained ground state, and the reverse order of reactivity for substrate having l-(4-trifluoromethyl)phenyl vs. that having 1-(3-trifluoromethyl

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