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2,6-DIKETO-15-CROWN-5 is a chemical compound characterized by its crown ether structure, which features five oxygen atoms and a central cavity. With a molecular formula of C12H24O6, 2,6-DIKETO-15-CROWN-5 is widely recognized for its selective complexing capabilities, particularly for alkali and alkaline earth metal cations. Its high affinity for potassium ions makes it a valuable asset in various applications, including separation and extraction processes, as well as in the development of ion-selective electrodes and sensors. Furthermore, the unique structure and molecular properties of 2,6-DIKETO-15-CROWN-5 have garnered interest for its potential use in drug delivery and catalysis.

63689-58-7

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63689-58-7 Usage

Uses

Used in Separation and Extraction Processes:
2,6-DIKETO-15-CROWN-5 is used as a selective complexing agent for the separation and extraction of alkali and alkaline earth metal cations, particularly potassium ions, due to its high affinity for these ions.
Used in Ion-Selective Electrodes and Sensors:
2,6-DIKETO-15-CROWN-5 is utilized in the development of ion-selective electrodes and sensors, where its selective complexing properties allow for the precise detection and measurement of specific metal cations in various environments.
Used in Drug Delivery Systems:
2,6-DIKETO-15-CROWN-5 is studied for its potential application in drug delivery, where its unique structure and molecular properties could be leveraged to improve the efficiency and targeting of therapeutic agents.
Used in Catalysis:
2,6-DIKETO-15-CROWN-5 is also being explored for its use in catalysis, where its ability to selectively complex with metal cations could enhance the efficiency of certain chemical reactions.
Used in Chemical Research:
2,6-DIKETO-15-CROWN-5 is employed in chemical research to study the interactions between metal cations and crown ethers, contributing to the understanding of supramolecular chemistry and the development of new materials and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63689-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,8 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63689-58:
(7*6)+(6*3)+(5*6)+(4*8)+(3*9)+(2*5)+(1*8)=167
167 % 10 = 7
So 63689-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O7/c11-9-7-15-8-10(12)17-6-4-14-2-1-13-3-5-16-9/h1-8H2

63689-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,7,10,13-pentaoxacyclopentadecane-2,6-dione

1.2 Other means of identification

Product number -
Other names -

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:63689-58-7 SDS

63689-58-7Downstream Products

63689-58-7Relevant academic research and scientific papers

Condensation of Diglycolic Acid Dichloride with Polyglycols. 5. An Improved Synthesis of Cyclic Polyether-Esters by Cyclization

Erk, Cakil

, p. 1083 - 1084 (2007/10/02)

An improved synthesis of oligocyclic (ether-ester)s by cyclization condensation of polyglycols with diglycolic acid dichloride in benzene/pyridine or dioxane/pyridine is reported. Keywords: Macrocyclic oligo(ether-ester)s

The Reduction of Crown Lactones to Crown Ethers

Ager, David J.,Sutherland, O.

, p. 248 - 249 (2007/10/02)

Crown lactones may be reduced to crown ethers using lithium aluminium hydride.

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