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Assay
97%
form
solid
bp
120-121 °C/1 mmHg (lit.)
mp
63-65 °C (lit.)
functional group
acyl chloride
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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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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Synthesis of poly [2] rotaxane by Sonogashira polycondensation.
Journal of Polymer Science Part A: Polymer Chemistry, 45(17), 4154-4160 (2007)
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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