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Benzenemethanol, 3-chloro-α-phenyl-α-(trifluoromethyl)-, 4-methylbenzenesulfonate is a complex organic chemical compound with the molecular formula C15H13ClF3O3S. It is a derivative of benzenemethanol, featuring a 3-chloro substitution on the benzene ring, an α-phenyl group, and a trifluoromethyl group. The compound is further characterized by the presence of a 4-methylbenzenesulfonate group, which is a sulfonate ester derived from 4-methylbenzenesulfonic acid. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly those that require a combination of halogen, phenyl, and trifluoromethyl functionalities. Its unique structure may also contribute to its reactivity and stability in various chemical reactions.

96235-97-1

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96235-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96235-97-1 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 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96235-97:
(7*9)+(6*6)+(5*2)+(4*3)+(3*5)+(2*9)+(1*7)=161
161 % 10 = 1
So 96235-97-1 is a valid CAS Registry Number.

96235-97-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Toluene-4-sulfonic acid 1-(3-chloro-phenyl)-2,2,2-trifluoro-1-phenyl-ethyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:96235-97-1 SDS

96235-97-1Downstream Products

96235-97-1Relevant 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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