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Benzoic acid-(2,2,2-trinitro-ethyl ester), also known as trinitroethyl benzoate, is a chemical compound with the molecular formula C9H7N3O7. It is an ester derivative of benzoic acid, where the hydroxyl group is replaced by a 2,2,2-trinitroethyl group. benzoic acid-(2,2,2-trinitro-ethyl ester) is characterized by its explosive properties due to the presence of three nitro groups, which make it highly sensitive to shock and heat. Trinitroethyl benzoate is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. It has been studied for its potential use in explosives and as a chemical intermediate in the synthesis of other nitro compounds. However, due to its hazardous nature, it is not widely used and requires careful handling and storage to prevent accidents.

843-66-3

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843-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 843-66-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 843-66:
(5*8)+(4*4)+(3*3)+(2*6)+(1*6)=83
83 % 10 = 3
So 843-66-3 is a valid CAS Registry Number.

843-66-3Downstream Products

843-66-3Relevant academic research and scientific papers

Ionic liquid-assisted synthesis of trinitroethyl esters

Sheremetev, Aleksei B.,Yudin, Igor L.,Suponitsky, Kirill Yu.

, p. 264 - 266 (2006)

The first, highly efficient esterification of 2,2,2-trinitroethanol with alkanoyl, cycloalkanoyl, aroyl and hetaroyl chloride promoted by simple ionic liquids is described; trinitroethyl esters were characterised by X-ray crystallography.

Sterically Hindered Carboxylic Acid Esters

Bagal,Ishchenko,Nikolaev

, p. 1731 - 1738 (2007/10/03)

Methods have been developed for preparation of esters formed by sterically hindered benzoic acids and various alcohols, which were difficult to obtain previously. The methods are based on the reaction of carbenium ions, generated from primary aliphatic N-nitroamines by the action of nitrous acid or Lewis acids, with carboxylic acid at the sterically accessible oxygen atom of the carboxy group. Reactions of nitrobenzoic acids and benzenepolycarboxylic acids with 2,2,2-trinitroethyl hydrogen sulfate provide an effective method for preparation of corresponding trinitroethyl esters.

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