:2-Iodobenzoic acid
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| Watchedfields = changed
| verifiedrevid = 477213655
| Name = 2-Iodobenzoic acid
| Reference =
| ImageFile = 2-Iodobenzoic acid.svg
| ImageSize = 120px
| PIN = 2-Iodobenzoic acid
| OtherNames = o-Iodobenzoic acid
|Section1={{Chembox Identifiers
| CASNo = 88-67-5
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 7Q00V80J7Q
| PubChem = 6941
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 6675
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 287979
| SMILES = O=C(O)c1ccccc1I
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 112424
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI=1S/C7H5IO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey=CJNZAXGUTKBIHP-UHFFFAOYSA-N
}}
|Section2={{Chembox Properties
| Formula = C7H5IO2
| MolarMass = 248.018 g/mol
| Appearance = white solid
| Density = 2.25 g/cm3
| MeltingPtC = 162
| BoilingPt =
| Solubility =
}}
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
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|Section7={{Chembox Hazards
| NFPA-H =
| NFPA-F =
| NFPA-R =
| ExternalSDS =
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| Section8 = {{Chembox Related
| OtherCompounds = 4-Iodobenzoic acid
}}
}}
2-Iodobenzoic acid, or o-iodobenzoic acid, is an isomer of iodobenzoic acid.{{Cite web |website=PubChem |title=2-Iodobenzoic acid |url=https://pubchem.ncbi.nlm.nih.gov/compound/6941 |access-date=2022-11-27 |language=en}} The synthesis of 2-iodobenzoic acid via the diazotization of anthranilic acid is commonly performed in university organic chemistry labs. One of its most common uses is as a precursor for the preparation of IBX and Dess–Martin periodinane, both used as mild oxidants.
Synthesis
2-Iodobenzoic acid can be synthesized by a Sandmeyer reaction: the diazotization of anthranilic acid followed by a reaction with iodide.
Image:Diazo Coupling Of Anthranilic Acid.png
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See also
References
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{{DEFAULTSORT:Iodobenzoic acid, 2-}}