Skip to Content
MilliporeSigma
All Photos(1)

Documents

206547

Sigma-Aldrich

4-Iodobenzoic acid

98%

Synonym(s):

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

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
IC6H4CO2H
CAS Number:
619-58-9
Molecular Weight:
248.02
Beilstein/REAXYS Number:
1860232
EC Number:
210-603-2
MDL number:
MFCD00002533
UNSPSC Code:
12352100
PubChem Substance ID:
24852407
NACRES:
NA.22

assay

98%

mp

270-273 °C (lit.)

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

2,5-Diiodobenzoic acid 97%

Sigma-Aldrich

107905

2,5-Diiodobenzoic acid

4-Iodobenzaldehyde 96%

Sigma-Aldrich

263826

4-Iodobenzaldehyde

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
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
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)
Zengyan Wei et al.
Nature communications, 5, 3870-3870 (2014-05-16)
The shape-controlled synthesis of nanoparticles was established in single-phase solutions by controlling growth directions of crystalline facets on seed nanocrystals kinetically; however, it was difficult to rationally predict and design nanoparticle shapes. Here we introduce a methodology to fabricate nanoparticles

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service