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Trifluoro-acetic acid 2,3,5,6-tetramethylphenyl ester is a complex organic compound characterized by its unique chemical structure. It is an ester derivative of trifluoroacetic acid, where the hydroxyl group of the acid is replaced by a 2,3,5,6-tetramethylphenyl group. trifluoro-acetic acid 2,3,5,6-tetramethylphenyl ester is known for its stability and reactivity, which can be attributed to the presence of the electron-withdrawing trifluoromethyl groups and the electron-donating methyl groups on the phenyl ring. It is often used in synthetic chemistry as a protecting group for alcohols and as a reagent in various organic transformations. The compound's properties, such as its lipophilicity and resistance to hydrolysis, make it a valuable tool in the synthesis of complex molecules and pharmaceuticals.

1799-88-8

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1799-88-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1799-88-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1799-88:
(6*1)+(5*7)+(4*9)+(3*9)+(2*8)+(1*8)=128
128 % 10 = 8
So 1799-88-8 is a valid CAS Registry Number.

1799-88-8Downstream Products

1799-88-8Relevant academic research and scientific papers

Remarkable effect of water on functionalization of the phenyl ring in methyl-substituted benzene derivatives with F-TEDA-BF4

Kralj, Petra,Zupan, Marko,Stavber, Stojan

, p. 3880 - 3888 (2006)

Various N-F reagents reacted with hexamethylbenzene (1) forming side chain substituted alkoxides or esters in protic solvents, Ritter type side chain functionalization was observed in acetonitrile in the presence of trifluoroacetic acid, while in aqueous

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