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Sigma-Aldrich

4-Iodbenzoylchlorid

97%

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About This Item

Lineare Formel:
IC6H4COCl
CAS-Nummer:
1711-02-0
Molekulargewicht:
266.46
EG-Nummer:
216-974-7
MDL-Nummer:
MFCD00001058
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24855184
NACRES:
NA.22

Assay

97%

Form

solid

bp

120-121 °C/1 mmHg (lit.)

mp (Schmelzpunkt)

63-65 °C (lit.)

SMILES String

ClC(=O)c1ccc(I)cc1

InChI

1S/C7H4ClIO/c8-7(10)5-1-3-6(9)4-2-5/h1-4H

InChIKey

NJAKCIUOTIPYED-UHFFFAOYSA-N

Verwandte Kategorien

Anwendung

4-Iodobenzoyl chloride has been used in:
  • modification of poly(allylamine), to make the polymer x-ray visible
  • preparation of series of N-(1-benzylpyrrolidin-3-yl)arylbenzamides, potential human dopamine D4 antagonists
  • preparation of [2] rotaxane monomer, for poly [2] rotaxane synthesis
  • synthesis of pyrroles from imines and acetylenes mediated by isocyanides versus palladium catalysis

Piktogramme

Corrosion
GHS05

Signalwort

Danger

H-Sätze

H314

Gefahreneinstufungen

Eye Dam. 1 - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Damia Mawad et al.
Nanotechnology, 21(33), 335603-335603 (2010-07-27)
Contrast agents are currently used in a variety of diagnostic imaging techniques, including computer tomography for early cancer detection. Radiopaque nanoparticles have recently been proposed as an alternative method to traditional contrast agents that may allow for long-term image tracking.
Synthesis of poly [2] rotaxane by Sonogashira polycondensation.
Sasabe H, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 45(17), 4154-4160 (2007)
Daniel J St Cyr et al.
Organic letters, 9(3), 449-452 (2007-01-26)
[reaction: see text] A direct synthesis of pyrroles from imines, acid chlorides, and alkynes mediated by isocyanides is reported. This reaction proceeds with a range of each of these three substrates, providing a method to generate families of pyrroles in
Ian Egle et al.
Bioorganic & medicinal chemistry letters, 14(19), 4847-4850 (2004-09-03)
A series of N-(1-benzylpyrrolidin-3-yl)arylbenzamides 8 has been prepared, and their structure-activity relationships studied. Potent ligands selective for human D(4) (hD(4)) over hD(2) and alpha(1) have been identified. One example was determined to be an antagonist in a cAMP assay, with
Ni Chen et al.
Journal of Asian natural products research, 22(5), 444-451 (2019-03-20)
A series of aromatic or long-chain chrysin derivatives (1-10) were synthesized by esterification of chrysin and acyl chloride. The chemical structures of these compounds were determined by mass spectrum (MS), 1H NMR, and 13C NMR spectra. Though aromatic chrysin derivatives
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