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550566

Sigma-Aldrich

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

98%

Synonym(s):

2,2′-Bipyridyl-4,4′-dicarboxylic acid

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About This Item

Empirical Formula (Hill Notation):
C12H8N2O4
CAS Number:
6813-38-3
Molecular Weight:
244.20
Beilstein:
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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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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