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5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 480434-20-6 Structure
  • Basic information

    1. Product Name: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine
    2. Synonyms: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine
    3. CAS NO:480434-20-6
    4. Molecular Formula:
    5. Molecular Weight: 358.248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 480434-20-6.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: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine(480434-20-6)
    11. EPA Substance Registry System: 5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,2’-bipyridine(480434-20-6)
  • 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: 480434-20-6(Hazardous Substances Data)

480434-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 480434-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,0,4,3 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 480434-20:
(8*4)+(7*8)+(6*0)+(5*4)+(4*3)+(3*4)+(2*2)+(1*0)=136
136 % 10 = 6
So 480434-20-6 is a valid CAS Registry Number.

480434-20-6Relevant articles and documents

Guest encapsulation and self-assembly of a cavitand-based coordination capsule

Haino, Takeharu,Kobayashi, Mutsumi,Fukazawa, Yoshimasa

, p. 3310 - 3319 (2006)

The synthesis and spectroscopic characterization of a cavitand-based coordination capsule 1·4 BF4 of nanometer dimensions is described. Encapsulation studies of large aromatic guests as well as aliphatic guests were performed by using 1/s

A new self-assembling capsule via metal coordination

Haino, Takeharu,Kobayashi, Mutsumi,Chikaraishi, Midori,Fukazawa, Yoshimasa

, p. 2321 - 2323 (2005)

A new octadentate cavitand forms a stable dimeric molecular capsule via metal-coordination, creating a large and elaborate three-dimensional cavity in which large aromatic guests are accommodated to form supramolecular complexes. The Royal Society of Chemistry 2005.

Lewis Acid–Base Interaction-Controlled ortho-Selective C?H Borylation of Aryl Sulfides

Li, Hong Liang,Kuninobu, Yoichiro,Kanai, Motomu

supporting information, p. 1495 - 1499 (2017/02/05)

An iridium/bipyridine-catalyzed ortho-selective C?H borylation of aryl sulfides was developed. High ortho-selectivity was achieved by a Lewis acid–base interaction between a boryl group of the ligand and a sulfur atom of the substrate. This is the first example of a catalytic and regioselective C?H transformation controlled by a Lewis acid–base interaction between a ligand and a substrate. The C?H borylation reaction could be conducted on a gram scale, and with a bioactive molecule as a substrate, demonstrating its applicability to late-stage regioselective C?H borylation. A bioactive molecule was synthesized from an ortho-borylated product by converting the boryl and methylthio groups of the product.

Purines bearing phenanthroline or bipyridine ligands and their RuII complexes in position 8 as model compounds for electrochemical DNA labeling - Synthesis, crystal structure, electrochemistry, quantum chemical calculations, cytostatic and antiviral activity

Vrabel, Milan,Hocek, Michal,Havran, Ludek,Fojta, Miroslav,Votruba, Ivan,Klepetarova, Blanka,Pohl, Radek,Rulisek, Lubomir,Zendlova, Lucie,Hobza, Pavel,Shih, I.-Hung,Mabery, Eric,Mackman, Richard

, p. 1752 - 1769 (2008/02/06)

A series of ethynyl- or (4-boronophenyl)bipyridines and -phenanthrolines were prepared as versatile building blocks for attachment of bidentate N-ligands to other molecules via cross-coupling reactions. Their complexation with Ru(bpy)2-Cl2 gave the corresponding RuII complexes. 9-Benzyladenine derivatives bearing the bipyridine or phenanthroline complexes in position 8, attached via a conjugate acetylene or phenylene linker were prepared by cross-coupling reactions of the ethynyl- or 4-boronophenylbipyridines and -phenanthrolines with 9-benzyl-8-bromoadenine. Their complexation with Ru(bpy)2Cl2 afforded the corresponding Ru complexes as model compounds for electrochemical DNA labeling. The same compounds were also prepared directly by cross-coupling of 9-benzyl-8-bromoadenine with Ru complexes of the alkynes and boronic acids. Both approaches are compared in terms of potential applications for labeling of nucleic acids. The crystal structures of two Ru complexes were determined by X-ray diffraction. The electrochemistry of the model purines bearing the phenanthroline or bipyridine ligands and the Ru complexes was studied by means of cyclic or square-wave voltammetry with carbon paste and mercury electrodes. The experimental redox potentials of the title compounds were compared with quantum chemical calculations. A very good agreement between experiment and theory was obtained, with a standard deviation of 0.13 V. It was shown that theoretical calculations can be of a limited predictive power for new Ru II complexes, though it was difficult to reproduce differences smaller than 0.05 V. Several compounds of this series exhibited a considerable cytostatic effect and activity against the hepatitis C virus (HCV). Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

Fullerene sensors based on calix[5]arene

Haino, Takeharu,Araki, Hiromi,Fujiwara, Yoshihisa,Tanimoto, Yoshifumi,Fukazawa, Yoshimasa

, p. 2148 - 2149 (2007/10/03)

A new class of fullerene sensors based on calix[5]arenes has produced the highly sensitive detection of C60 and C70.

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