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206547

4-Iodobenzoic acid

Name: 4-Iodobenzoic acid
Brand: ALDRICH

98%

Synonym(s):

4-Iodobenzoic acid, Iodobenzene-4-carboxylic acid, p-Iodobenzenecarboxylic acid, p-Iodobenzoic acid

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About This Item

Linear Formula:

IC₆H₄CO₂H

CAS Number:

619-58-9

Molecular Weight:

248.02

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24852407

EC Number:

210-603-2

Beilstein/REAXYS Number:

1860232

MDL number:

MFCD00002533

Assay:

98%

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Properties

Quality Level

200

assay

98%

mp

270-273 °C (lit.)

functional group

carboxylic acid, iodo

SMILES string

OC(=O)c1ccc(I)cc1

InChI

1S/C7H5IO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)

InChI key

GHICCUXQJBDNRN-UHFFFAOYSA-N

Description

Application

4-Iodobenzoic acid was used in the synthesis of [hydroxy(4-carboxyphenyl)iodonium]ion in situ that helps in the cleavage of a variety of alkenes.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Oxidative cleavage of alkenes using an in situ generated iodonium ion with oxone as a terminal oxidant.

Prem P Thottumkara et al.

Organic letters, 12(24), 5640-5643 (2010-11-18)

A facile and operationally convenient catalytic procedure for oxidative cleavage of alkenes is described. In situ formed [hydroxy(4-carboxyphenyl)iodonium]ion, 2, from the oxidation of 4-iodobenzoic acid, 1, has been shown to facilitate the cleavage of a variety of alkenes in presence

Comparing Positively and Negatively Charged Distonic Radical Ions in Phenylperoxyl Forming Reactions.

Peggy E Williams et al.

Journal of the American Society for Mass Spectrometry, 29(9), 1848-1860 (2018-06-06)

In the gas phase, arylperoxyl forming reactions play a significant role in low-temperature combustion and atmospheric processing of volatile organic compounds. We have previously demonstrated the application of charge-tagged phenyl radicals to explore the outcomes of these reactions using ion

Self-assembling Properties of an N-Heterocyclic Carbene-based Metallosurfactant: Pd-Coordination Induced Formation of Reactive Interfaces in Water.

Toshiaki Taira et al.

Journal of oleo science, 67(9), 1107-1115 (2018-09-04)

In this study, an N-heterocyclic carbene (NHC)-based metallosurfactant (MS), NHC-PdMS, was synthesized, where Pd(II) was bound to the NHC framework via a robust Pd-carbene bond with NEt3 as a co-ligand. Surface tension measurements revealed that the critical micelle concentration (CMC)

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Global Trade Item Number

SKU	GTIN
206547-5G	04061838768711
206547-25G	04061838768704