4-Iodobenzoyl chloride

4-Iodobenzoyl chloride Structure
4-Iodobenzoyl chloride structure
Common Name 4-Iodobenzoyl chloride
CAS Number 1711-02-0 Molecular Weight 266.464
Density 1.9±0.1 g/cm3 Boiling Point 310.6±0.0 °C at 760 mmHg
Molecular Formula C7H4ClIO Melting Point 62-66 °C
MSDS Chinese USA Flash Point 120.7±22.6 °C
Symbol GHS05
GHS05
Signal Word Danger

Synthesis and Photophysical Studies of Calixarene-Based Alkynylplatinum(II) Terpyridine Complexes with Various Receptor Sites for Colorimetric and Luminescence Sensing of Anions.

Chemistry 22 , 3738-49, (2016)

A series of mononuclear and dinuclear platinum(II) terpyridine complexes with amide-, sulfonamide-, and urea-containing ligands (1-9) has been successfully designed and synthesized, and their photophysical and anion-binding properties have been studied. The a...

Direct synthesis of pyrroles from imines, alkynes, and acid chlorides: an isocyanide-mediated reaction.

Org. Lett. 9 , 449, (2007)

[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 hig...

Synthesis and characterization of novel radiopaque poly(allyl amine) nanoparticles.

Nanotechnology 21(33) , 335603, (2010)

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 a...

N-(1-Benzylpyrrolidin-3-yl)arylbenzamides as potent and selective human dopamine D4 antagonists.

Bioorg. Med. Chem. Lett. 14(19) , 4847-50, (2004)

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 an...

Synthesis of poly [2] rotaxane by Sonogashira polycondensation. Sasabe H, et al.

J. Polym. Sci. A Polym. Chem. 45(17) , 4154-60, (2007)