206547
4-Iodobenzoic acid
98%
Sinonimo/i:
4-Iodobenzoic acid, Iodobenzene-4-carboxylic acid, p-Iodobenzenecarboxylic acid, p-Iodobenzoic acid
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About This Item
Formula condensata:
IC6H4CO2H
Numero CAS:
Peso molecolare:
248.02
Beilstein:
1860232
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
98%
Punto di fusione
270-273 °C (lit.)
Gruppo funzionale
carboxylic acid
iodo
Stringa SMILE
OC(=O)c1ccc(I)cc1
InChI
1S/C7H5IO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)
GHICCUXQJBDNRN-UHFFFAOYSA-N
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Applicazioni
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.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
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
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