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Iodonium, phenyl-2-thienyl-bromide, also known as 2-(phenylsulfonyl)thiazolium bromide, is a chemical compound with the molecular formula C12H8BrNOS2. It is a derivative of iodonium salts, which are widely used as electrophilic iodinating agents in organic synthesis. This specific compound features a phenyl group attached to a 2-thienyl ring, with a bromine atom and a sulfonate group connected to the iodonium center. It is a pale yellow solid and is soluble in organic solvents. Due to its reactivity, it is commonly used in the synthesis of various iodinated compounds, such as aryl iodides and heteroaryl iodides, which are important intermediates in pharmaceutical and agrochemical industries. The compound is also known for its stability and ease of handling, making it a preferred choice for iodination reactions in research and industrial settings.

2665-62-5

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2665-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2665-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2665-62:
(6*2)+(5*6)+(4*6)+(3*5)+(2*6)+(1*2)=95
95 % 10 = 5
So 2665-62-5 is a valid CAS Registry Number.

2665-62-5Downstream Products

2665-62-5Relevant academic research and scientific papers

One-pot preparations of diaryliodonium bromides from iodoarenes and arenes, with sodium perborate as the oxidant

Kryska, Anna,Skulski, Lech

, p. 875 - 880 (2007/10/03)

This paper reports a one-pot synthesis of the title bromides from both activated and deactivated iodoarenes which are first oxidized with anhydrous NaBO3·H2O/Ac2O/conc.H2SO 4 liquid mixtures, then coupled in situ with benzene and activated arenes and, finally, precipitated out with a KBr solution; this method is easy, cheap, safe and fairly effective.

A short-cut synthesis of diaryliodonium bromides followed by oxidative anion metatheses

Kazmierczak,Skulski

, p. 1027 - 1032 (2007/10/02)

This paper reports a one-pot synthesis of the title bromides (in 20-88% crude yields) from iodoarenes oxidized with the CrO3/AcOH/Ac2O/H2SO4 liquid mixture, then coupled in situ with arenes and, finally, precipitated out with a KBr solution. Similarly, diaryliodonium perchlorates and iodides are obtained in 40-89% crude yields. Oxidative anion metatheses in the crude title bromides produce the respective pure diaryliodonium tetrafluoroborates, tosylates, trifluoroacetates, hydrosulfates, nitrates, and chlorides in 57-80% yields. These new preparative procedures are easier and shorter than many earlier methods.

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