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(2-azanidylcyclohexyl)azanide; nickel is a coordination complex formed by the interaction of (2-azanidylcyclohexyl)azanide, a chemical compound containing a cyclohexyl group and two azanide groups, and nickel, a silvery-white lustrous metal with a wide range of applications. This complex can be used in various industrial and research applications due to its unique properties.

53748-60-0

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53748-60-0 Usage

Uses

Used in Chemical Reactions:
(2-azanidylcyclohexyl)azanide; nickel is used as a catalyst in chemical reactions for its ability to facilitate and speed up the process. The presence of the azanide groups in the ligand allows for strong coordination with the nickel, enhancing the catalytic activity.
Used in Coordination Chemistry:
(2-azanidylcyclohexyl)azanide; nickel is used as a ligand in coordination chemistry for its ability to form stable complexes with various metal ions. The cyclohexyl group provides steric hindrance, which can influence the geometry and properties of the resulting complexes.
Used in Material Science:
(2-azanidylcyclohexyl)azanide; nickel is used in the development of new materials with unique properties, such as magnetic, electronic, or optical characteristics. The combination of the organic ligand and the metal center can lead to the formation of coordination polymers or other supramolecular structures with potential applications in various fields.
Used in Pharmaceutical Industry:
(2-azanidylcyclohexyl)azanide; nickel may be used in the pharmaceutical industry for the development of new drugs or drug delivery systems. The coordination complexes formed by (2-azanidylcyclohexyl)azanide; nickel and nickel could have potential therapeutic applications, such as targeting specific biological processes or improving the bioavailability of certain drugs.
Used in Environmental Applications:
(2-azanidylcyclohexyl)azanide; nickel can be used in environmental applications, such as the remediation of contaminated sites or the treatment of wastewater. The complex may have the ability to bind and remove heavy metals or other pollutants from the environment, providing a potential solution for environmental challenges.

Check Digit Verification of cas no

The CAS Registry Mumber 53748-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53748-60:
(7*5)+(6*3)+(5*7)+(4*4)+(3*8)+(2*6)+(1*0)=140
140 % 10 = 0
So 53748-60-0 is a valid CAS Registry Number.

53748-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-azanidylcyclohexyl)azanide,nickel

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:53748-60-0 SDS

53748-60-0Upstream product

53748-60-0Downstream Products

53748-60-0Relevant academic research and scientific papers

Solid-phase thermal square-planar-to-octahedral isomeric transformation of nickel(II) complexes containing 1,2-cyclohexanediamines

Ihara, Yoshinori,Fukuda, Yutaka,Sone, Kozo

, p. 3745 - 3750 (2008/10/08)

New examples of thermal square-planar (low-spin)-to-octahedral (high-spin) isomeric transformations were discovered and studied in the thermal reactions of bis(dl- or meso-1,2-cyclohexanediamine)nickel(II) complexes, [Ni(dl- or ms-chxn)2]X2 (X = Cl, Br, NO3), in the solid phase. These transformations proceeded endothermically and were accompanied by a reversible thermochromism from yellow to violet-blue. Obvious differences in the reactivity between the ms-chxn complexes and the ms-chxn ones were observed. They indicate that this type of reaction (and the stability of the square-planar species) is strongly dominated by the steric effect of the substituent groups in the coordinated diamines. The enthalpy changes for these endothermic transformations were found to be small (8 kJ/mol). The activation energies for them were also estimated.

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