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Cycloheptyl trifluoroacetate is an organic compound with the chemical formula C10H15F3O2. It is a derivative of cycloheptane, a seven-carbon cyclic hydrocarbon, with a trifluoroacetyl group (CF3CO-) attached to one of its carbon atoms. cycloheptyl trifluoroacetate is characterized by its unique structure, which combines the cyclic nature of cycloheptane with the electron-withdrawing properties of the trifluoroacetyl group. Cycloheptyl trifluoroacetate is used in various chemical reactions and synthetic processes, particularly in the preparation of pharmaceuticals and agrochemicals, due to its ability to influence the reactivity and selectivity of the molecules it is part of. Its stability and unique electronic properties make it a valuable intermediate in organic synthesis.

777-58-2

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777-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 777-58-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 777-58:
(5*7)+(4*7)+(3*7)+(2*5)+(1*8)=102
102 % 10 = 2
So 777-58-2 is a valid CAS Registry Number.

777-58-2Downstream Products

777-58-2Relevant academic research and scientific papers

Cobalt catalyzed carboxylation reaction of saturated hydrocarbons with CO in the presence of K2S2O8 and TFA under mild conditions

Asadullah, Mohammad,Taniguchi, Yuki,Kitamura, Tsugio,Fujiwara, Yuzo

, p. 8867 - 8871 (1999)

Cobalt(II) acetate (Co(OAc)2) has been found to be an efficient catalyst for the carboxylation reaction of saturated hydrocarbons with CO to yield the corresponding carboxylic acids in high yields in the presence of K2S2O8 and CF3COOH. About 89.5% conversion of propane is obtained in this reaction. The activation parameters of the reaction of propane have been determined by Arrhenius and Eyring plots.

Heterolytic decarboxylation involving acyltrifluoroacetyl peroxide intermediates

Krasutsky, Pavel A.,Kolomitsyn, Igor V.,Botov, Evgenij M.,Carlson, Robert M.,Semenova, Irina G.,Fokin, Andrey A.

, p. 8687 - 8691 (2007/10/03)

Selective carboxylic acid decarboxylation was elaborated. Generation of acyltrifluoroacetyl peroxides from carboxylic peracids and trifluoroacetyl anhydride (Method A), as well as from trifluoroperacetic acid and acyltrifluoroacetyl anhydride (Method B), leads to simultaneous peroxide decomposition into the corresponding alkyltrifluoroacetates. DFT computations, as well as experimental data, support an acid-catalyzed heterolytic mechanism for acyltrifluoroacetyl peroxide decomposition.

Synthesis of carboxylic acids through the formation of C-C bond between saturated hydrocarbons and CO in the presence of Mg/K2S2O8/TFA system

Asadullah, Mohammad,Kitamura, Tsugio,Fujiwara, Yuzo

, p. 449 - 450 (2007/10/03)

Magnesium powder (Mg) promoted the carboxylation reaction of saturated hydrocarbons with carbon monoxide (CO) in the presence of potassium peroxodisulfate (K2S2O8) in trifluoroacetic acid (TFA) to yield the corresponding carboxylic acids and alkyl trifluoroacetates. About 80% conversion of cyclohexane was achieved when 5 mmol of magnesium, 5 mmol of potassium peroxodisulfate, 3 mL of TFA, 1 mmol of cyclohexane, 50 atm of CO were used at 80 °C for 30 h.

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