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CS-W001157 4
Total: USD 88.00

(Acetato-κO)[[2,2'-[(1R,2R)-1,2-cyclohexanediylbis[(nitrilo-κN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-κO]](2-)]cobalt

  • CAS No. 201870-82-8

  • Cat. No. CS-0855633
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

(Acetato-κO)[[2,2'-[(1R,2R)-1,2-cyclohexanediylbis[(nitrilo-κN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-κO]](2-)]cobalt|CS-0855633

Structure of 201870-82-8

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General Information

  • CAS No. 201870-82-8
  • Cat. No. CS-0855633
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₈H₅₅CoN₂O₄
  • Molecular Weight 662.79
  • Synonym(s) None
  • SMILES CC([O-][Co+3]123[N]([C@@]4([H])[C@](CCCC4)([H])[N]2=CC5=CC(C(C)(C)C)=CC(C(C)(C)C)=C5[O-]3)=CC6=CC(C(C)(C)C)=CC(C(C)(C)C)=C6[O-]1)=O

Description

This cobalt complex features a sterically shielded, electron-rich ligand framework derived from a bulky bisphenol scaffold with nitrile and acetate donors. The coordinated cobalt center resides in a rigid, multidentate environment that enhances stability and modulates redox behavior, enabling controlled catalytic activity under ambient conditions.

Application

This cobalt complex serves as a robust catalyst for C–H functionalization and oxidative coupling reactions, leveraging its stable tridentate ligand framework. The sterically shielded phenolate donors enhance redox stability and selectivity, while the acetato bridge facilitates reversible coordination. Its bench-stable nature and tolerance to diverse functional groups enable reliable use in multistep syntheses and heterocycle construction.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07,GHS08
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H351
Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   N/A
  • LogP   N/A
  • H_Acceptors   N/A
  • H_Donors   N/A
  • Rotatable_Bonds   N/A

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