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4-Methoxybenzhydryl trifluoroacetate is a chemical compound with the molecular formula C16H15F3O3. It is a derivative of benzhydryl, which is a diphenylmethane structure, and features a 4-methoxy group attached to the benzene ring. The trifluoroacetate group is a trifluoromethyl ester of acetic acid, which is known for its strong electron-withdrawing properties. 4-methoxybenzhydryl trifluoroacetate is often used in organic synthesis as a protecting group for amines due to its stability and ease of removal under mild conditions. It is also employed in the synthesis of various pharmaceuticals and agrochemicals, where its reactivity and selectivity can be advantageous. The compound is typically synthesized through the reaction of 4-methoxybenzhydrol with trifluoroacetic anhydride. Its physical properties include a low melting point and it is often used in its solid form for chemical reactions.

441-54-3

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441-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 441-54-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 441-54:
(5*4)+(4*4)+(3*1)+(2*5)+(1*4)=53
53 % 10 = 3
So 441-54-3 is a valid CAS Registry Number.

441-54-3Relevant academic research and scientific papers

Kinetics of the solvolyses of benzhydryl derivatives: Basis for the construction of a comprehensive nucleofugality scale

Denegri, Bernard,Streiter, Andre,Juric, Sandra,Ofial, Armin R.,Kronja, Olga,Mayr, Herbert

, p. 1648 - 1656 (2007/10/03)

A series of 21 benzhydrylium ions (diarylmethylium ions) are proposed as reference electrofuges for the development of a general nucleofugality scale, where nucleofugality refers to a combination of leaving group and solvent. A total of 167 solvolysis rate constants of benzhydrylium tosylates, bromides, chlorides, trifluoroacetates, 3,5-dinitrobenzoates, and 4-nitroben-zoates, two-thirds of which have been determined during this work, were subjected to a least-squares fit according to the correlation equation log k 25°C = Sf(Nf + Ef), where s f and Nf are nucleofuge-specific parameters and E f is an electrofuge-specific parameter. Although nucleofuges and electrofuges characterized in this way cover more than 12 orders of magnitude, a single set of the parameters, namely sf, Nf, and E f, is sufficient to calculate the solvolysis rate constants at 25°C with an accuracy of ± 16%. Because sf ≈ 1 for all nucleofuges, that is, leaving group/ solvent combinations, studied so far, qualitative discussions of nucleofugality can be based on Nf.

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