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α-(4-Bromophenylmercapto)phenylacetic acid is a chemical compound characterized by its unique structure, which features a phenyl ring attached to an acetic acid group, with a 4-bromophenylmercapto group (a 4-bromophenylthio group) connected to the alpha carbon of the acetic acid. α-<4-Brom-phenylmercapto>-phenyl-essigsaeure is known for its potential applications in the synthesis of various organic compounds and pharmaceuticals, particularly those involving sulfur-containing moieties. Its specific properties, such as reactivity and stability, make it a valuable intermediate in chemical research and development.

93533-99-4

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93533-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93533-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,3 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93533-99:
(7*9)+(6*3)+(5*5)+(4*3)+(3*3)+(2*9)+(1*9)=154
154 % 10 = 4
So 93533-99-4 is a valid CAS Registry Number.

93533-99-4Downstream Products

93533-99-4Relevant academic research and scientific papers

Direct α-Chalcogenation of Aliphatic Carboxylic Acid Equivalents

Gupta, Aniket,Rahaman, Ajijur,Bhadra, Sukalyan

, p. 6164 - 6168 (2019/08/20)

A novel approach to α-chalcogenation of aliphatic carboxylic acids has been developed by means of transforming them as the corresponding benzazoles. The catalyst system, consisting of CuI, DMSO, and a base, operates through a unique mechanism t

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