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[2,2'-Bipyridine]-4,4'-dicarboxylic acid, also known as 4,4'-dicarboxy-2,2'-bipyridine, is a fine chemical that is a carboxylated derivative of 2,2'-bipyridine. This organic compound has the formula C12H8N2O4 and is characterized by the presence of two pyridine rings interconnected by a single bond with two carboxylic acids at the 4-position respectively. Its structure allows it to function as a bidentate ligand, especially in coordination chemistry, where it binds transition metals.

117330-40-2

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117330-40-2 Usage

Uses

Used in Coordination Chemistry:
[2,2'-Bipyridine]-4,4'-dicarboxylic acid is used as a bidentate ligand for the formation of coordination polymers and organometallic complexes. Its ability to bind transition metals makes it a valuable component in the development of materials with specific catalytic or optical properties.
Used in Catalyst Preparation:
[2,2'-Bipyridine]-4,4'-dicarboxylic acid is used as a precursor in the synthesis of catalysts, particularly those that require the coordination of transition metals. Its role in the formation of active sites on catalysts contributes to their efficiency in various chemical reactions.
Used in Optical Device Manufacturing:
[2,2'-Bipyridine]-4,4'-dicarboxylic acid is used as a component in the production of optical devices, such as light-emitting diodes (LEDs) and solar cells. Its coordination with metals can lead to the creation of materials with desired optical properties, enhancing the performance of these devices.
Used in Research and Development:
[2,2'-Bipyridine]-4,4'-dicarboxylic acid is used as a reagent in academic and industrial research settings. Its unique structure and reactivity make it a valuable tool for studying the properties of coordination compounds and exploring new applications in materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 117330-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,3,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117330-40:
(8*1)+(7*1)+(6*7)+(5*3)+(4*3)+(3*0)+(2*4)+(1*0)=92
92 % 10 = 2
So 117330-40-2 is a valid CAS Registry Number.

117330-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(4-methoxycarbonyl-6-methylpyridin-2-yl)-6-methylpyridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 6,6'-dimethyl-4,4'-dicarbomethoxy-2,2'-bipyridine

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:117330-40-2 SDS

117330-40-2Relevant articles and documents

A General, Multimetallic Cross-Ullmann Biheteroaryl Synthesis from Heteroaryl Halides and Heteroaryl Triflates

Dibenedetto, Tarah A.,Kang, Kai,Loud, Nathan L.,Weix, Daniel J.

supporting information, p. 21484 - 21491 (2022/01/03)

Despite their importance to medicine and materials science, the synthesis of biheteroaryls by cross-coupling remains challenging. We describe here a new, general approach to biheteroaryls: the Ni-and Pd-catalyzed multimetallic cross-Ullmann coupling of he

Lanthanide-series compound and preparation method and application thereof

-

, (2016/10/24)

The invention provides a lanthanide-series compound and a preparation method and an application thereof; the lanthanide-series compound has the chemical structural formula described in the description. The lanthanide-series compound has no inversion center, is beneficial for the compound to generate higher-brightness fluorescence, and enables a strongest emission peak to be used in a fluorescence analysis peak of time-resolved fluorescence immunoassay; and at the same time, the compound has relatively strong stability, and still can be used for marking and testing after being placed for a certain time.

AROMATIC COMPOUNDS AND METAL COMPLEXES THEREOF

-

, (2012/12/13)

Provided are aromatic compounds and metal complexes thereof which may be useful treating various forms of proliferative diseases, such as cancer. In some instances, the metal complexes thereof are relatively stable, and may be suitable for oral administra

An element of surprise - Efficient copper-functionalized dye-sensitized solar cells

Bessho, Takeru,Constable, Edwin C.,Graetzel, Michael,Hernandez Redondo, Ana,Housecroft, Catherine E.,Kylberg, William,Nazeeruddin,Neuburger, Markus,Schaffner, Silvia

body text, p. 3717 - 3719 (2009/02/07)

Dye-sensitized solar cells with carboxylate-derivatized {Cu IL2} complexes are surprisingly efficient and offer a long-term alternative approach to ruthenium-functionalized systems. The Royal Society of Chemistry.

Synthesis and Characterisation of the Sodium and Lithium Cryptates of Macrobicyclic Ligands Incorporating Pyridine, Bipyridine, and Biisoquinoline Units

Alpha, Beatrice,Anklam, Elke,Deschenaux, Robert,Lehn, Jean-Marie,Pietraskiewicz, Marek

, p. 1042 - 1052 (2007/10/02)

Synthetic procedures have been developed for the preparation of sodium and lithium cryptates of the macrobicyclic ligands 1-11 containing pyridine, bipyridine, and biisoquinoline groups.They involve stepwise construction of the bicyclic system as well as direct macrobicyclisation procedures (Scheme 1) and give access to both symmetrical and dissymmetrical structures.Marked cation template effects have been found that facilitate the cyclisation processes.The ligands 1-11 were isolated as their cryptates with Na+ or Li+ cations.

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