41070-12-6

Basic information

• Product Name: 3-IODOCINNAMIC ACID
• Synonyms: 3-IODOCINNAMIC ACID;3-(3-IODOPHENYL)ACRYLIC ACID;RARECHEM AL BK 0709
• CAS NO: 41070-12-6
• Molecular Formula: C₉H₇IO₂
• Molecular Weight: 274.06
• Product Categories: Aromatic Cinnamic Acids, Esters and Derivatives;Acids & Esters;Iodine Compounds
• Mol File: 41070-12-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 3-IODOCINNAMIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-IODOCINNAMIC ACID(41070-12-6)
• EPA Substance Registry System: 3-IODOCINNAMIC ACID(41070-12-6)

Safety Data

• Hazardous Substances Data: 41070-12-6(Hazardous Substances Data)

Usage

General Description

3-Iodocinnamic acid is an organic compound that consists of a cinnamic acid with an iodine substituent at the 3-position. It is a white crystalline solid with a molecular formula of C9H7IO2 and a molecular weight of 274.06 g/mol. 3-Iodocinnamic acid is commonly used as a synthetic intermediate in organic chemistry and is also employed in the production of pharmaceuticals and agrochemicals. It is known for its ability to undergo various chemical reactions, including substitution, addition, and oxidation processes. Additionally, this compound has potential applications in the field of materials science, particularly in the development of functionalized polymers and other advanced materials.

Upstream product

• 1664-56-8 m-aminocinnamic acid 
• 696-41-3 m-iodobenzaldehyde 
• 108-24-7 acetic anhydride 
• 14473-91-7 3-Bromocinnamic acid 

Downstream Products

• 59114-92-0 (E)‐3‐(3‐iodophenyl)acryloyl chloride 
• 81069-39-8 (E)-ethyl 3-(3-iodophenyl)acrylate 
• 68034-75-3 3-(3-iodophenyl)propanoic acid 
• 59114-91-9 3-iodo-N-ethylcinnamamide 
• 14755-02-3 3-hydroxy-trans-cinnamic acid 

Relevant articles and documents

COPPER-CATALYZED FORMATION OF CARBON-HETEROATOM AND CARBON-CARBON BONDS

One aspect of the present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-sulfur bond between the sulfur atom of a thiol moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper(II)-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-carbon bond between the carbon atom of cyanide ion and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In another embodiment, the present invention relates to a copper-catalyzed method of transforming and aryl, heteroaryl, or vinyl iodide. Yet another embodiment of the present invention relates to a tandem method, which may be practiced in a single reaction vessel, wherein the first step of the method involves the copper-catalyzed formation of an aryl, heteroaryl, or vinyl iodide from the corresponding aryl, heteroaryl, or vinyl chloride or bromide; and the second step of the method involves the copper-catalyzed formation of an aryl, heteroaryl, or vinyl nitrile, amide or sulfide from the aryl, heteroaryl, or vinyl iodide formed in the first step.