13064-64-7

Usage

Uses

2,5-Diiodobenzene-1,4-diol can be used to treat viral diseases.

Upstream product

• 150-78-7 1,4-dimethoxybezene 
• 51560-21-5 1,4-diiodo-2,5-dimethoxybenzene 
• 25245-35-6 1-iodo-2,4-dimethoxybenzene 
• 123-31-9 hydroquinone 
• 87905-74-6 hydroquinone bis(methoxymethyl)ether 
• 916226-09-0 2,5-bis(methoxymethoxy)-1,4-diiodobenzene 
• 915706-87-5 2,5-diiodo-1,4-bis-(hydroxymethyl)benzene 

Downstream Products

• 357396-86-2 4-(hexyloxy)-2,5-diiodophenol 
• 250608-58-3 1,4-diiodo-2,5-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene 
• 911307-60-3 2,5-diiodo-4-octyloxyphenol 
• 377093-03-3 diethyl 2,2'-((2,5-diiodo-1,4-phenylene)bis(oxy))diacetate 
• 864227-82-7 1,4-bis((11-undecanol)oxy)-2,5-diiodobenzene 
• 505065-16-7 2,2'-(2,5-diiodo-1,4-phenylene)bis(oxy)diethanoic acid 
• 475265-41-9 C₃₀H₄₈I₂O₆ 
• 921869-63-8 1,4-diiodo-2,5-bis[(S)-3,7-dimethyloctyloxy]benzene 
• 929803-60-1 2,5-bis{[4-(tert-butyl)benzyl]oxy}-1,4-diiodobenzene 
• 929803-61-2 2,5-bis[(3,5-bis{[4-(tert-butyl)benzyl]oxy}benzyl)oxy]-1,4-diiodobenzene 
• 929803-63-4 2,5-bis{[3,5-bis(tert-butyl)benzyl]oxy}-1,4-diiodobenzene 
• 929803-64-5 2,5-bis[(3,5-bis{[3,5-bis(tert-butyl)benzyl]oxy}benzyl)oxy]-1,4-diiodobenzene 
• 211809-85-7 2,5-bis[(isoamyl)oxy]-1,4-diiodobenzene 
• 1014621-93-2 1,4-diiodo-2,5-bis-[(S)-(+)-2-methylbutanoxy]benzene 

Relevant academic research and scientific papers

Fluorometric, water-based sensors for the detection of nerve gas G mimics DMMP, DCP and DCNP

Water-based ZnII bisterpyridine systems were used as fluorometric sensors for the detection of the nerve gas G mimics DMMP, DCP and DCNP. Analyte concentrations in the range of 10-7 to 10-6 M are detectable in solution. Th

Two Functional Porous Metal-Organic Frameworks Constructed from Expanded Tetracarboxylates for Gas Adsorption and Organosulfurs Removal

Two fof-type porous metal-organic frameworks (MOFs), [Cu2(bdfdpa)(H2O)2]·8DMF·2H2O (JLU-Liu29) and [Cu2(btadpa)(H2O)2]·7DMF·8H2O (JLU-Liu30) (H4bdfdpa = 5,5

Synthesis and functionalization of a highly fluorescent and completely water-soluble poly(para-phenyleneethynylene) copolymer for bioconjugation

Bioconjugation of a highly fluorescent water-soluble poly(para-phenyleneethynylene) (PPE) copolymer with ionic and non-ionic side chains is achieved by means of chain-end modification, providing a design principle for biosensor development. The Royal Soci

Amplified fluorescence quenching and electroluminescence of a cationic poly(p-phenylene-co-thiophene) polyelectrolyte

A water-soluble conjugated polymer was developed that displays significant fluorescence quenching (25% quenching of polymer's fluorescence at quencher concentrations of 500 nM) and forms well-defined multilayer structures via electrostatic deposition. The

Amplified quenching in metal-organic conjugated polymers

The luminescence from conjugated polyelectrolytes that contain pendant metal complex units is quenched very efficiently by oppositely charged electron acceptors.

How Large Can We Build a Cyclic Assembly? Impact of Ring Size on Chelate Cooperativity in Noncovalent Macrocyclizations

Self-assembled systems rely on intramolecular cooperative effects to control their growth and regulate their shape, thus yielding discrete, well-defined structures. However, as the size of the system increases, cooperative effects tend to dissipate. We analyze here this situation by studying a set of oligomers of different lengths capped with guanosine and cytidine nucleosides, which associate in cyclic tetramers by complementary Watson–Crick H-bonding interactions. As the monomer length increases, and thus the number of C(sp)–C(sp2) σ-bonds in the π-conjugated skeleton, the macrocycle stability decreases due to a notable reduction in effective molarity (EM), which has a clear entropic origin. We determined the relationship between EM or ΔS and the number of σ-bonds, which allowed us to predict the maximum monomer lengths at which cyclic species would still assemble quantitatively, or whether the cyclic species would not able to compete at all with linear oligomers over the whole concentration range.

A new conjugated polymer-based combination probe for ATP detection using a multisite-binding and FRET strategy

A new conjugated polymer-based ratiometric combination probe was constructed for adenosine triphosphate detection by taking advantage of a multisite-binding and fluorescence resonance energy transfer strategy. The method is rapid and highly selective, whi

Molecular Wire Effects in Phenyleneethynylene Oligomers: Surprising Insights

The synthesis and quenching behavior of a series of water-soluble, carboxylate-carrying phenyleneethynylene oligomers—monomer to tetramer—and their polymers are reported; their quenching behavior with different test analytes (paraquat, lead salts, mercury

A highly selective fluorescent sensor for Hg2+ based on the water-soluble poly(p-phenyleneethynylene)

The conjugated polymer P-1 could be synthesized by the polymerization of 4,7-diethynyl-benzo[2,1,3]thiadiazole (M-1) and 1,4-bis[3'-(N,N-diethylamino)-1'-oxapropyl]-2,5-diiodobenzene (M-2) via Pd-catalyzed Sonogashira reaction. The water-soluble conjugate

COMPOUND, DETECTION MATERIAL AND DETECTION METHOD OF SUGAR COMPOUND USING THE SAME

PROBLEM TO BE SOLVED: To provide a novel compound suitable for detection of a sugar compound, and detection means of the sugar compound using the same. SOLUTION: There is provided a compound represented by the general formula (A1) or (B1). Ar1 is a substituent and/or an aromatic ring which may have a hetero group in a ring; each Ar2 each independently is an aromatic ring which may have a substituent, Ar3 is an aromatic ring which has at least one -B(OH)2 and may have a substituent; R1 is H or a C1 to 20 alkyl group or an alkyloxy group which may have a hetero atom in a middle of a carbon chain; n is an integer of 1 to 5; and a bond represented by a combination of a double bond and a dash line each independently is a double bond or a triple bond. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT