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1562-95-4

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1562-95-4 Usage

Description

DI-2-PYRIDYL KETOXIME, also known as di-2-pyridyl ketone oxime, is a chemical compound with the ability to form complexes with various metal ions. It is characterized by its hexanuclear clusters with rare manganese oxidation-state combinations and its capability to form neutral binuclear and cationic trinuclear, pentanuclear, or hexanuclear complexes in copper chemistry.

Uses

Used in Metal Assay:
DI-2-PYRIDYL KETOXIME is used as a standard in the metal assay for the determination of cobalt. It serves as a metal-complexing agent, which is essential for accurate measurements and analysis in this application.
Used in Chemical Research:
In the field of chemical research, DI-2-PYRIDYL KETOXIME is employed as a metal-complexing agent. Its ability to form complexes with various metal ions, such as manganese and copper, makes it a valuable tool for studying the properties and behavior of these metals in different chemical reactions and processes.
Used in Analytical Chemistry:
DI-2-PYRIDYL KETOXIME is also utilized in analytical chemistry as a reagent for the detection and quantification of metal ions. Its complexing properties allow for the selective identification and measurement of specific metal ions in samples, which is crucial for various analytical applications.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, DI-2-PYRIDYL KETOXIME may also have potential applications in the pharmaceutical industry. Its metal-complexing properties could be harnessed for the development of new drugs or drug delivery systems that target specific metal ions, which are often involved in various diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 1562-95-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1562-95:
(6*1)+(5*5)+(4*6)+(3*2)+(2*9)+(1*5)=84
84 % 10 = 4
So 1562-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H9N3O/c15-14-11(9-5-1-3-7-12-9)10-6-2-4-8-13-10/h1-8,12H

1562-95-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H58153)  2,2'-Dipyridyl ketoxime, 98%   

  • 1562-95-4

  • 2g

  • 1376.0CNY

  • Detail
  • Alfa Aesar

  • (H58153)  2,2'-Dipyridyl ketoxime, 98%   

  • 1562-95-4

  • 10g

  • 5504.0CNY

  • Detail
  • Aldrich

  • (161705)  Di-2-pyridylketoneoxime  98%

  • 1562-95-4

  • 161705-1G

  • 844.74CNY

  • Detail

1562-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name DI-2-PYRIDYL KETOXIME

1.2 Other means of identification

Product number -
Other names 2,2′-Dipyridyl ketoxime

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:1562-95-4 SDS

1562-95-4Relevant articles and documents

Synthesis and transition metal coordination chemistry of a novel hexadentate bispidine ligand

Comba, Peter,Rudolf, Henning,Wadepohl, Hubert

, p. 2724 - 2736 (2015)

Reported is the new bispidine-derived hexadentate ligand L (L = 3-(2-methylpyridyl)-7-(bis-2-methylpyridyl)-3,7-diazabicyclo[3.3.1]nonane) with two tertiary amine and four pyridine donor groups. This ligand can form heterodinuclear and mononuclear complexes and, in the mononuclear compounds discussed here, the ligand may coordinate as a pentadentate ligand, with one of the bispyridinemethane-based pyridine groups un- or semi-coordinated, or as a hexadentate ligand, leading to a pentagonal pyramidal coordination geometry or, with an additional monodentate ligand, to a heptacoordinate pentagonal bipyramidal structure. The solution and solid state data presented here indicate that, with the relatively small CuII and high-spin FeII ions the fourth pyridine group is only semi-coordinated for steric reasons and, with the larger high-spin MnII ion genuine heptacoordination is observed but with a relatively large distortion in the pentagonal equatorial plane. This journal is

Hybrid organic-inorganic materials from di-(2-pyridyl)methylamine-palladium dichloride complex as recoverable catalysts for Suzuki, Heck and Sonogashira reactions

Trilla, Montserrat,Pleixats, Roser,Man, Michel Wong Chi,Bied, Catherine,Moreau, Joel J. E.

, p. 577 - 590 (2008)

Hybrid silica materials containing the di-(2-pyridyl)methylamine-palladium dichloride complex, prepared by sol-gel cogelification, are efficient recyclable catalysts for Suzuki (aryl bromides and chlorides), Heck (aryl bromides) and Sonogashira reactions (aryl iodides and bromides). Formation of palladium(0) nanoparticles is observed in the Suzuki and Heck reactions but not in the Sonogashira coupling.

Interplay Between Steric and Electronic Effects: A Joint Spectroscopy and Computational Study of Nonheme Iron(IV)-Oxo Complexes

Mukherjee, Gourab,Alili, Aligulu,Barman, Prasenjit,Kumar, Devesh,Sastri, Chivukula V.,de Visser, Sam P.

, p. 5086 - 5098 (2019)

Iron is an essential element in nonheme enzymes that plays a crucial role in many vital oxidative transformations and metabolic reactions in the human body. Many of those reactions are regio- and stereospecific and it is believed that the selectivity is guided by second-coordination sphere effects in the protein. Here, results are shown of a few engineered biomimetic ligand frameworks based on the N4Py (N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine) scaffold and the second-coordination sphere effects are studied. For the first time, selective substitutions in the ligand framework have been shown to tune the catalytic properties of the iron(IV)-oxo complexes by regulating the steric and electronic factors. In particular, a better positioning of the oxidant and substrate in the rate-determining transition state lowers the reaction barriers. Therefore, an optimum balance between steric and electronic factors mediates the ideal positioning of oxidant and substrate in the rate-determining transition state that affects the reactivity of high-valent reaction intermediates.

Aromatic-ring-containing compound, preparation method thereof, pharmaceutical composition and application thereof

-

Paragraph 0602-0606, (2018/08/03)

The invention discloses an aromatic-ring-containing compound, a preparation method thereof, a pharmaceutical composition and application. The present invention provides the aromatic-ring-containing compound represented by a formula 1, a pharmaceutically acceptable salt thereof, a stereoisomer thereof, a tautomer thereof or a solvate thereof, and the aromatic-ring-containing compound can be effectively bounded to bromodomains of BRD4, BRD3, BRD2, and BRDT in BET family to regulate transcription of downstream gene c-myc and related target genes of the c-myc so as to regulate downstream signalingpathways to play specific roles including treatment of diseases such as inflammatory diseases, cancer, and AIDS. Some of the compounds have high activity, and have good cell activity and metabolic stability, so that the compounds can be an effective drug for treating tumors.

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