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1,4-DIHYDROXY-2,5-DIIODOBENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13064-64-7

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13064-64-7 Usage

Uses

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

Check Digit Verification of cas no

The CAS Registry Mumber 13064-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,6 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13064-64:
(7*1)+(6*3)+(5*0)+(4*6)+(3*4)+(2*6)+(1*4)=77
77 % 10 = 7
So 13064-64-7 is a valid CAS Registry Number.

13064-64-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-diiodobenzene-1,4-diol

1.2 Other means of identification

Product number -
Other names 1,4-Benzenediol,2,5-diiodo

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13064-64-7 SDS

13064-64-7Relevant academic research and scientific papers

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

Wild, Andreas,Winter, Andreas,Hager, Martin D.,Schubert, Ulrich S.

, p. 964 - 966 (2012)

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

Luo, Xiaolong,Kan, Liang,Li, Xiang,Sun, Libo,Li, Guanghua,Zhao, Jun,Li, Dong-Sheng,Huo, Qisheng,Liu, Yunling

, p. 7301 - 7307 (2016)

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

Lee, Kangwon,Cho, Jae Cheol,DeHeck, Jennifer,Kim, Jinsang

, p. 1983 - 1985 (2006)

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

Ramey, Michael B.,Hiller, JerI'Ann,Rubner, Michael F.,Tan, Chunyan,Schanze, Kirk S.,Reynolds, John R.

, p. 234 - 243 (2005)

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

Liu, Yao,Jiang, Shujun,Schanze, Kirk S.

, p. 650 - 651 (2003)

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

Montoro-García, Carlos,Mayoral, María J.,Chamorro, Raquel,González-Rodríguez, David

, p. 15649 - 15653 (2017)

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

Zhao, Qi,Zhang, Ziqi,Tang, Yanli

, p. 9414 - 9417 (2017)

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

Hergert, Marcel,Bender, Markus,Seehafer, Kai,Bunz, Uwe H. F.

, p. 3132 - 3135 (2018)

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)

Li, Jie,Meng, Jie,Huang, Xiaobo,Cheng, Yixiang,Zhu, Chengjian

, p. 3425 - 3430 (2010)

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

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Paragraph 0092; 0093, (2020/02/22)

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

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