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10 G
$89.58
100 G
$424.00
About This Item
Linear Formula:
I3C6H2CO2H
CAS Number:
Molecular Weight:
499.81
Beilstein/REAXYS Number:
1955088
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
$89.58
List Price$94.30Save 5%Web-Only Promotion
Available to ship onMay 01, 2025Details
Request a Bulk Order
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assay
98%
mp
220-222 °C (lit.)
solubility
methanol: soluble 5%
functional group
carboxylic acid
iodo
SMILES string
OC(=O)c1cc(I)cc(I)c1I
InChI
1S/C7H3I3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)
InChI key
ZMZGFLUUZLELNE-UHFFFAOYSA-N
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Application
2,3,5-Triiodobenzoic acid has been used in the synthesis of aromatic iodine containing vinylic monomer, 2-methacryloyloxyethyl(2,3,5-triiodobenzoate) used in preparing radiopaque polymers[1].
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The auxin transport inhibitor 2, 3, 5-triiodobenzoic acid (TIBA) inhibits the stimulation of in vitro lateral root formation and the colonization of the tap-root cortex of Norway spruce (Picea abies) seedlings by the ectomycorrhizal fungus Laccaria bicolor.
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The Effect of 2,4-Dichlorophenoxyacetic Acid and 2,3,5-Triiodobenzoic Acid on the Transport of Indoleacetic Acid.
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Cucumber (Cucumis sativus) seedlings grown in a horizontal position develop a specialized protuberance (or peg) on the lower side of the transition zone between the hypocotyl and the root. This occurs by suppressing peg formation on the upper side via
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