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1,3-di-(n-butoxy)-4,6-diiodobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 259222-95-2 Structure
  • Basic information

    1. Product Name: 1,3-di-(n-butoxy)-4,6-diiodobenzene
    2. Synonyms: 1,3-di-(n-butoxy)-4,6-diiodobenzene
    3. CAS NO:259222-95-2
    4. Molecular Formula:
    5. Molecular Weight: 474.121
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 259222-95-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,3-di-(n-butoxy)-4,6-diiodobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-di-(n-butoxy)-4,6-diiodobenzene(259222-95-2)
    11. EPA Substance Registry System: 1,3-di-(n-butoxy)-4,6-diiodobenzene(259222-95-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 259222-95-2(Hazardous Substances Data)

259222-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 259222-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,2,2 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 259222-95:
(8*2)+(7*5)+(6*9)+(5*2)+(4*2)+(3*2)+(2*9)+(1*5)=152
152 % 10 = 2
So 259222-95-2 is a valid CAS Registry Number.

259222-95-2Relevant articles and documents

Synthesis and anion binding ability of metacyclophane-based cyclic thioureas

Tobe, Yoshito,Sasaki, Shin-Ichi,Mizuno, Masaaki,Naemura, Koichiro

, p. 835 - 836 (1998)

Cyclophanes having two thiourea groups were synthesized and their anion binding ability was examined by titration method using 1H-NMR spectroscopy. Strong and selective anion binding of the preorganized cyclic receptors was observed in the gene

Synthesis and characterization of a luminescent and fully rigid tetrakisimidazolium macrocycle

Zhou, Hongjun,Wang, Zhi,Gao, Chao,You, Jingsong,Gao, Ge

, p. 1832 - 1834 (2013/03/14)

A fully rigid tetrakisimidazolium macrocycle was synthesized in good yield for the first time through direct [2+2] cyclization. The structure was characterized by NMRs, MS and X-ray diffraction analysis. This cationic, fluorescent macrocycle with four hyd

Supramolecular assemblies and redox modulation of pyromellitic diimide-based cyclophane via noncovalent interactions with naphthol

Kato, Shin-Ichiro,Matsumoto, Taisuke,Ideta, Keiko,Shimasaki, Toshiaki,Goto, Kenta,Shinmyozu, Teruo

, p. 4723 - 4733 (2007/10/03)

This paper reports the electroscopic and electrochemical properties of [2 + 2] pyromellitic diimide-based cyclophane 1 as well as acyclic N,N′-bis(2-methoxybenzyl)pyromellitic diimide 2 and the clathrate compounds formed by 1. Compound 1 was synthesized b

Synthesis and anion-selective complexation of cyclophane-based cyclic thioureas

Sasaki, Shin-ichi,Mizuno, Masaaki,Naemura, Koichiro,Tobe, Yoshito

, p. 275 - 283 (2007/10/03)

Cyclic thiourea derivatives having three different types of cyclophane structure, ortho-meta, meta-meta, and meta-para, and a lariat-type thiourea, were synthesized, and their anion-binding ability was examined. The association constants for the complexation between the receptors and several anions in DMSO-d6 were measured by the titration method using 1H NMR spectroscopy. All receptors, except for the meta-para cyclophane, exhibit selective binding to the dihydrogenphosphate anion, which is stronger than that of the acyclic reference compound. The lariat-type receptor binds anions even more strongly than the cyclic receptors which do not possess the third binding site.

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