I7675
2-Iodobenzoic acid
98%
Synonym(s):
o-Iodobenzoic acid, IBA
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About This Item
Linear Formula:
IC6H4CO2H
CAS Number:
Molecular Weight:
248.02
Beilstein:
1861406
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
mp
160-162 °C (lit.)
SMILES string
OC(=O)c1ccccc1I
InChI
1S/C7H5IO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)
InChI key
CJNZAXGUTKBIHP-UHFFFAOYSA-N
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Application
2-Iodobenzoic acid can be used as a reactant in the synthesis of oligo(m-phenylene ethynylenes),[1] (±)-lycoricidine[2] and various detoxifiers of organophosphorus nerve agents.[3][4] Additionally, it is used as a precursor in the preparation of oxidizing reagents like 2-iodoxybenzoic acid (IBX) and Dess-Martin periodinane (DMP).[5][6]
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Functionalized polymer nanofibre membranes for protection from chemical warfare stimulants.
Ramaseshan R, et al.
Nanotechnology, 17(12), 2947-2947 (2006)
Organoiodinane oxyanions as reagents for the cleavage of a reactive phosphate.
Moss RA, et al.
The Journal of Organic Chemistry, 51(22), 4303-4307 (1986)
A user-friendly entry to 2-iodoxybenzoic acid (IBX).
Frigerio M, et al.
The Journal of Organic Chemistry, 64(12), 4537-4538 (1999)
The Dess-Martin Periodinane: 1, 1, 1-Triacetoxy-1, 1-Dihydro-1, 2-Benziodoxol-3 (1H)-One
Boeckman RK, et al.
Organic Syntheses, 64(12), 141-141 (2000)
Backbone-rigidified oligo (m-phenylene ethynylenes).
Yang X, et al.
Journal of the American Chemical Society, 126(10), 3148-3162 (2004)
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