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Iodonium, (4-methoxyphenyl)(4-nitrophenyl)-, bromide (1:1) is a chemical compound with the formula C13H10BrIN2O3. It is a salt formed from the reaction of iodonium cation and bromide anion. The compound consists of a central iodine atom bonded to two phenyl rings, one of which is substituted with a methoxy group (-OCH3) and the other with a nitro group (-NO2). The presence of these functional groups imparts specific reactivity and properties to the compound. This iodonium salt is often used as a reagent in organic synthesis, particularly in electrophilic aromatic substitution reactions, due to its ability to act as a source of electrophilic iodine. The 1:1 ratio in the name indicates that one mole of iodonium cation is combined with one mole of bromide anion in the compound.

4072-45-1

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4072-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4072-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4072-45:
(6*4)+(5*0)+(4*7)+(3*2)+(2*4)+(1*5)=71
71 % 10 = 1
So 4072-45-1 is a valid CAS Registry Number.

4072-45-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxyphenyl)-(4-nitrophenyl)iodanium,bromide

1.2 Other means of identification

Product number -
Other names Iodonium,(p-methoxyphenyl)(p-nitrophenyl)-bromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4072-45-1 SDS

4072-45-1Downstream Products

4072-45-1Relevant 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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