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550566

Sigma-Aldrich

2,2′-Bipyridine-4,4′-dicarboxylic acid

98%

Sinónimos:

2,2′-Bipyridyl-4,4′-dicarboxylic acid

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About This Item

Fórmula empírica (notación de Hill):
C12H8N2O4
Número de CAS:
6813-38-3
Peso molecular:
244.20
Beilstein/REAXYS Number:
212894
MDL number:
MFCD00015430
UNSPSC Code:
12162002
PubChem Substance ID:
24879125
NACRES:
NA.23

Quality Level

100

assay

98%

SMILES string

OC(=O)c1ccnc(c1)-c2cc(ccn2)C(O)=O

InChI

1S/C12H8N2O4/c15-11(16)7-1-3-13-9(5-7)10-6-8(12(17)18)2-4-14-10/h1-6H,(H,15,16)(H,17,18)

InChI key

FXPLCAKVOYHAJA-UHFFFAOYSA-N

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Application


  • Enhanced catalysis of CO2 cycloaddition at ambient pressure through rational design of interpenetrating ZnII/LnIII heterometallic coordination polymers: This study highlights the use of 2,2′-bipyridine-4,4′-dicarboxylic acid in the synthesis of ZnII/LnIII coordination polymers, which exhibit enhanced catalytic performance for CO2 cycloaddition at ambient pressure (Chuasaard et al., 2024).

  • Immobilization of a new copper (II) complex dye with multi-walled carbon nanotubes and functional simulation in dye-sensitized solar cell: This research describes the synthesis of a new ligand using 2,2′-bipyridine-4,4′-dicarboxylic acid combined with multiwalled carbon nanotubes for potential applications in dye-sensitized solar cells (Shahbaznejad et al., 2023).

  • Impact of Anchoring Groups on the Photocatalytic Performance of Iridium (III) Complexes and Their Toxicological Analysis: The study investigates the photocatalytic performance and toxicological analysis of Iridium (III) complexes using 2,2′-bipyridine-4,4′-dicarboxylic acid as an anchoring unit (Yao et al., 2024).

  • Phosphonate-based iron complex for a cost-effective and long cycling aqueous iron redox flow battery: This paper discusses the use of 2,2′-bipyridine-4,4′-dicarboxylic acid in the development of a high redox potential Fe-Dcbpy/CN catholyte for iron redox flow batteries (Nambafu et al., 2024).

  • 2, 2′-bipyridine-4, 4′-dicarboxylic acid ligand engineered CsPbBr3 perovskite nanocrystals for enhanced photoluminescence quantum yield with stable display properties: This article explores the use of 2,2′-Bipyridine-4,4′-dicarboxylic acid to improve the optical properties of CsPbBr3 perovskite nanocrystals for display applications (Kumar et al., 2024).


pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
WXBF3985V
WXBF1301V
WXBD7775V
WXBD7081V
MKCM2264

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Bo Zheng et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(30), E3987-E3996 (2015-06-28)
New dyads consisting of a strongly absorbing Bodipy (dipyrromethene-BF2) dye and a platinum diimine dithiolate (PtN2S2) charge transfer (CT) chromophore have been synthesized and studied in the context of the light-driven generation of H2 from aqueous protons. In these dyads
Xiang Huang et al.
The Analyst, 140(17), 6015-6024 (2015-07-21)
An efficient aptasensor was developed in which graphene oxide (GO) was employed as an indicator for both electrochemical impedance spectroscopy and electrochemiluminescence (ECL) signal generation. The aptasensor was fabricated by self-assembling the ECL probe of a thiolated adenosine triphosphate binding
Nathan R Rose et al.
Journal of medicinal chemistry, 51(22), 7053-7056 (2008-10-24)
The dynamic methylation of histone lysyl residues plays an important role in biology by regulating transcription, maintaining genomic integrity, and by contributing to epigenetic effects. Here we describe a variety of inhibitor scaffolds that inhibit the human 2-oxoglutarate-dependent JMJD2 subfamily
Maxence Urbani et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(45), 16252-16265 (2015-09-12)
The detailed synthesis and characterization of four ruthenium(II) complexes [RuLL'(NCS)2 ] is reported, in which L represents a 2,2'-bipyridine ligand functionalized at the 4,4' positions with benzo[1,2-b:4,5-b']dithiophene derivatives (BDT) and L' is 2,2'-bipyridine-4,4'-dicarboxylic acid unit (dcbpy) (NCS=isothiocyanate). The reaction conditions

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