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About This Item
Linear Formula:
IC6H4COCl
CAS Number:
Molecular Weight:
266.46
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
form
solid
bp
120-121 °C/1 mmHg (lit.)
mp
63-65 °C (lit.)
functional group
acyl chloride
iodo
SMILES string
ClC(=O)c1ccc(I)cc1
InChI
1S/C7H4ClIO/c8-7(10)5-1-3-6(9)4-2-5/h1-4H
InChI key
NJAKCIUOTIPYED-UHFFFAOYSA-N
Application
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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Journal of Polymer Science Part A: Polymer Chemistry, 45(17), 4154-4160 (2007)
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
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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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