17352-25-9

Usage

Uses

Used in Organic Synthesis:
3,5-Diiodobenzaldehyde is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, facilitating the creation of a wide range of organic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3,5-Diiodobenzaldehyde serves as an intermediate, playing a crucial role in the synthesis of different pharmaceuticals. Its presence in the production process is essential for the development of new drugs and medicines.
Used in Chemical Industry:
3,5-Diiodobenzaldehyde is utilized in the chemical industry for the synthesis of a variety of organic compounds, contributing to the diversity of chemical products available for various applications.

InChI:InChI=1/C7H4I2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H

Upstream product

• 14266-19-4 3,5‐diiodobenzoic acid methyl ester 
• 626-44-8 1,3,5-Triiodobenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 2122-61-4 4-amino-3,5-diiodobenzoic acid 
• 619-45-4 4-methoxycarbonyl aniline 
• 131755-87-8 methyl 4-amino-3,5-diiodobenzoate 
• 49617-79-0 1,3-diiodo-5-methylbenzene 
• 64662-57-3 2,6-diiodo-4-methylaniline 
• 106-49-0 p-toluidine 
• 53279-79-1 (3,5-diiodophenyl)methanol 
• 19094-48-5 3,5-diiodobenzoic acid 
• 535-87-5 3.5-diaminobenzoic acid 

Downstream Products

• 183862-90-0 2-(3,5-Diiodo-phenyl)-4,4,5,5-tetramethyl-imidazolidine-1,3-diol 
• 1211509-45-3 1-(2,2-dibromovinyl)-3,5-diiodobenzene 
• 875444-08-9 (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-one 
• 875446-37-0 anacetrapib 
• 1499179-50-8 (Z)-ethyl 3-(3,5-diiodophenyl)acrylate 
• 1499179-15-5 (Z)-3-(3,5-diiodophenyl)acrylic acid 
• 153390-73-9 3,5‐bis((trimethylsilyl)ethynyl)benzaldehyde 
• 153390-76-2 3,5-bis-(ethynyl)benzaldehyde 

Relevant academic research and scientific papers

A rigid metallohexameric macrocycle composed of endo- and exo-cyclic bisterpyridine-metal complexes

Synthesis of terpyridine-based building blocks has allowed the self-assembly of a nanosized metallomacrocycle with precisely positioned, peripheral metal complexes. Construction of the precursors included the assembly of a heteroleptic bisterpyridine-Ru(ii) complex possessing a diiodoaryl moiety that was subsequently reacted with two equivalents of 4′-ethynyl-2, 2′:6′,2′′-terpyridine via a Pd(0)-catalyzed Sonagashira coupling, to generate the requisite monomer with two, 120°-juxtaposed metal coordination sites. Addition of one equivalent of Fe(ii) to one equivalent of the bisligand afforded the metallocycle with 12 metals [6 internal Fe(ii) ions and 6 external Ru(ii) ions] measuring ca. 7 nm in diameter.

Conjugated oligoyne-bridged [60]fullerene molecular dumbbells: Syntheses and thermal and morphological properties

Chemical Equation Presented A series of linear and star-shaped π-conjugated oligomer hybrids (2-5) composed of an oligoyne core, ranging from 1,3-butadiyne to 1,3,5,7,9,11-dodecahexayne, and fullerenyl end-capping groups has been synthesized and studied.

Phenylene alkylene dendrons with site-specific incorporated fluorescent pyrene probes

This report deals with the synthesis and the spectroscopic properties of two second generation (G2) dendrons with site-specific incorporated phenyl pyrene derivatives as solvatochromic fluorescent probes. The generations that do not carry the probe are eq

Design, synthesis, and photodynamics of light-harvesting arrays comprised of a porphyrin and one, two, or eight boron-dipyrrin accessory pigments

Light-harvesting arrays containing one, two, or eight boron-dipyrrin (BDPY) pigments and one porphyrin (free base or Zn chelate) have been synthesized using a modular building block approach. The reaction of pyrrole and 4-(BDPY)benzaldehyde or 3,5-bis(BDP

Synthesis and magnetic behaviour of polyradical: Poly(1,3-phenyleneethynylene) with π-toporegulated pendant stable aminoxyl and imine N-oxide-aminoxyl radicals

The palladium-catalysed polycondensation of N-tert-butyl-N-(3,5-diethynylphenyl)aminoxyl with 2-(3,5-diiodophenyl)-4,4,5,5-tetramethyl-3-oxido-2-imidazolin-3-ium-l-yloxyl in pyridine-triethylamine at room temperature afforded poly(l,3-phenyleneethynylene)

2-phenyl-carbapenems

Carbapenems of the formula STR1 are useful intermediates to antibacterial agents.