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Tert-butyl 4-bromobenzoperoxoate is a chemical compound with the molecular formula C10H12BrO3. It is a colorless to pale yellow crystalline solid, often used as a reagent in organic synthesis. tert-butyl 4-bromobenzoperoxoate is a derivative of benzoperoxoic acid, where the hydrogen atom at the 4-position is replaced by a bromine atom, and the tert-butyl group is attached to the oxygen atom. Tert-butyl 4-bromobenzoperoxoate is known for its reactivity, particularly in the oxidation of alkenes to epoxides, and is also used in the preparation of various organic compounds. It is important to handle tert-butyl 4-bromobenzoperoxoate with care due to its potential reactivity and sensitivity to heat and light.

2123-95-7

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2123-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2123-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2123-95:
(6*2)+(5*1)+(4*2)+(3*3)+(2*9)+(1*5)=57
57 % 10 = 7
So 2123-95-7 is a valid CAS Registry Number.

2123-95-7Relevant academic research and scientific papers

Microfluidic Synthesis of tert-Butyl Peresters via KI-Catalyzed Oxidative Coupling of Methyl Arenes and tert-Butyl Hydroperoxide

Hua, Jiawei,Guo, Shiyu,Yang, Zhao,Fang, Zheng,Guo, Kai

, p. 1633 - 1637 (2017)

A green and efficient organic-aqueous two-phase reaction route for the synthesis of tert-butyl peresters by KI-catalyzed C-H oxidation of methyl arenes in a microfluidic chip reactor has been developed. Moreover, a series of tert-butyl perester products were obtained in moderate to good yields under metal-free conditions. A scale-up continuous flow system was constructed to verify the application of this method.

A Woven Supramolecular Metal-Organic Framework Comprising a Ruthenium Bis(terpyridine) Complex and Cucurbit[8]uril: Enhanced Catalytic Activity toward Alcohol Oxidation

Li, Zhan-Ting,Liu, Yi,Wang, Hui,Wang, Ze-Kun,Xu, Zi-Yue,Zhang, Dan-Wei,Zhang, Yun-Chang

, p. 1498 - 1503 (2020/08/05)

The self-assembly of a diamondoid woven supramolecular metal–organic framework wSMOF-1 has been achieved from intertwined [Ru(tpy)2]2+ (tpy=2,2′,6′,2′′-terpyridine) complex M1 and cucurbit[8]uril (CB[8]) in water, where the intermolecular dimers formed by the appended aromatic arms of M1 are encapsulated in CB[8]. wSMOF-1 exhibits ordered pore periodicity in both water and the solid state, as confirmed by a combination of 1H NMR spectroscopy, UV-vis absorption, isothermal titration calorimetry, dynamic light scattering, small angle X-ray scattering and selected area electron diffraction experiments. The woven framework has a pore aperture of 2.1 nm, which allows for the free access of both secondary and primary alcohols and tert-butyl hydroperoxide (TBHP). Compared with the control molecule [Ru(tpy)2]Cl2, the [Ru(tpy)2]2+ unit of wSMOF-1 exhibits a remarkably higher heterogeneous catalysis activity for the oxidation of alcohols by TBHP in n-hexane. For the oxidation of 1-phenylethan-1-ol, the yield of acetophenone was increased from 10 percent to 95 percent.

Bu4NI-catalyzed construction of tert-butyl peresters from alcohols

Zhang, Hui,Dong, Dao-Qing,Hao, Shuang-Hong,Wang, Zu-Li

, p. 8465 - 8468 (2016/02/09)

A new method for the synthesis of tert-butyl peresters directly from available alcohols catalyzed by Bu4NI at room temperature in an aqueous system was developed. Additionally, allylic esters could also be obtained by combing this method and Kharasch-Sosnovsky reaction via a two-step one-pot procedure.

Synthesis of tert-butyl peresters from aldehydes by Bu4NI- catalyzed metal-free oxidation and its combination with the Kharasch-Sosnovsky reaction

Wei, Wei,Zhang, Chao,Xu, Yuan,Wan, Xiaobing

supporting information; experimental part, p. 10827 - 10829 (2011/11/05)

A new tert-butyl peresters synthesis directly from aldehydes and TBHP was developed via Bu4NI-catalyzed aldehyde C-H oxidation. Mechanistic studies suggest that the protocol proceeds via a radical process. Combining the method with the Kharasch-Sosnovsky reaction offers a practical approach for the synthesis of allylic esters from simple aldehydes and alkenes via a two-step one-pot procedure.

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