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2‐bromo‐1,3‐diiodo‐5‐(trifluoromethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1123215-52-0

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1123215-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1123215-52-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,3,2,1 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1123215-52:
(9*1)+(8*1)+(7*2)+(6*3)+(5*2)+(4*1)+(3*5)+(2*5)+(1*2)=90
90 % 10 = 0
So 1123215-52-0 is a valid CAS Registry Number.

1123215-52-0Relevant academic research and scientific papers

Electrochemical Generation of Hypervalent Bromine(III) Compounds

Francke, Robert,Mohebbati, Nayereh,Sokolovs, Igors,Suna, Edgars

, p. 15832 - 15837 (2021)

In sharp contrast to hypervalent iodine(III) compounds, the isoelectronic bromine(III) counterparts have been little studied to date. This knowledge gap is mainly attributed to the difficult-to-control reactivity of λ3-bromanes as well as to their challenging preparation from the highly toxic and corrosive BrF3 precursor. In this context, we present a straightforward and scalable approach to chelation-stabilized λ3-bromanes by anodic oxidation of parent aryl bromides possessing two coordinating hexafluoro-2-hydroxypropanyl substituents. A series of para-substituted λ3-bromanes with remarkably high redox potentials spanning a range from 1.86 V to 2.60 V vs. Ag/AgNO3 was synthesized by the electrochemical method. We demonstrate that the intrinsic reactivity of the bench-stable bromine(III) species can be unlocked by addition of a Lewis or a Br?nsted acid. The synthetic utility of the λ3-bromane activation is exemplified by oxidative C?C, C?N, and C?O bond forming reactions.

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