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(1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane is a chiral compound characterized by the presence of two amino groups and two pyridinylcarbonyl groups attached to a cyclohexane ring. This unique structure endows it with distinctive properties and a wide range of applications in various fields of chemistry.

201551-23-7

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201551-23-7 Usage

Uses

Used in Coordination Chemistry:
(1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane is utilized as a ligand for forming stable complexes with transition metal ions. Its ability to chelate with these metal ions makes it a valuable component in coordination chemistry, particularly in catalytic processes.
Used in Asymmetric Catalysis:
In the field of asymmetric catalysis, (1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane is employed as a chiral ligand to induce enantioselectivity in chemical reactions. This application is crucial for the synthesis of enantiomerically pure compounds, which are essential in pharmaceuticals and agrochemicals.
Used in Metal Ion Extraction:
(1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane is also used in metal ion extraction processes. Its chelating properties allow for the selective extraction of metal ions from complex mixtures, which is important in environmental remediation and the purification of metal-containing solutions.
Used in the Synthesis of Coordination Polymers:
In the synthesis of coordination polymers, (1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane serves as a building block for creating complex, multi-dimensional structures with potential applications in materials science, such as in catalysis, gas storage, and molecular electronics.
Used in Organic and Inorganic Chemistry Research:
The unique structure and chiral nature of (1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane make it an important tool in both organic and inorganic chemistry research. It is used to explore new reaction mechanisms, develop novel synthetic methods, and investigate the properties of metal complexes.

Check Digit Verification of cas no

The CAS Registry Mumber 201551-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,5,5 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 201551-23:
(8*2)+(7*0)+(6*1)+(5*5)+(4*5)+(3*1)+(2*2)+(1*3)=77
77 % 10 = 7
So 201551-23-7 is a valid CAS Registry Number.

201551-23-7 Well-known Company Product Price

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  • Aldrich

  • (677523)  (1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane  97%

  • 201551-23-7

  • 677523-100MG

  • 1,157.13CNY

  • Detail
  • Aldrich

  • (677523)  (1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane  97%

  • 201551-23-7

  • 677523-500MG

  • 4,362.93CNY

  • Detail

201551-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-N,N'-(1R,2R)-1,2-diaminocyclohexylaminodi(2-pyridinanilide)

1.2 Other means of identification

Product number -
Other names (1R,2R)-(-)-1,2-BIS[(2-PYRIDINYLCARBONYL)AMINO]CYCLOHEXANE

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:201551-23-7 SDS

201551-23-7Downstream Products

201551-23-7Relevant articles and documents

Chiral bis-pyridinium salts as novel stereoselective catalysts for the metal-free diels-alder cycloaddition of α,β-unsaturated aldehydes

Genoni, Andrea,Benaglia, Maurizio,Puglisi, Alessandra,Rossi, Sergio

, p. 1926 - 1929 (2011)

The synthesis of enantiomerically pure C2-symmetric bis-pyridinium salts was realized through a simple condensation of 2-pyridyl-carboxyaldehydes with a chiral diamine. The catalytic properties of such novel compounds were preliminarily studied

New chiral diamide ligands: synthesis and application in allylic alkylation

Bateman, Lorraine,Breeden, Simon W.,O'Leary, Patrick

, p. 391 - 396 (2008/09/19)

A new family of chiral diamide ligands has been designed and synthesised. These ligands have been successfully applied to an asymmetric allylic substitution reaction. A palladium complex of one of the diamide ligands achieved enantioselectivities of up to 93% in the allylic alkylation of 1,3-diphenyl-3-acetoxyprop-1-ene.

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