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CS-W001157 4
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(OC-6-42)-Bis[[2,3-butanedione 2,3-di(oximato-κN)](1-)]chloro(4-methoxypyridine-κN)cobalt

  • CAS No. 1574577-65-3

  • Cat. No. CS-0642566
  • Purity≥98%
  • MDL No.None

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

(OC-6-42)-Bis[[2,3-butanedione 2,3-di(oximato-κN)](1-)]chloro(4-methoxypyridine-κN)cobalt|CS-0642566

Structure of 1574577-65-3

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General Information

  • CAS No. 1574577-65-3
  • Cat. No. CS-0642566
  • Purity ≥98%
  • MDL No. None
  • Storage RT, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₁ClCoN₅O₅
  • Molecular Weight 433.73
  • Synonym(s) None
  • SMILES Cl[Co]123([N]4=C(C)C(C)=[N]1O[H]O[N]2=C(C)C(C)=[N]3O[H]O4)[N]5=CC=C(OC)C=C5

Description

This cobalt complex features a bis-oximate chelating ligand system coordinated to a cobalt center, with a 4-methoxypyridine moiety enhancing solubility and stability. The structure integrates two 2,3-butanedione oximate units that form robust five-membered rings around the metal, enabling selective coordination in catalytic and redox applications.

Application

This cobalt complex serves as a stable, bench-accessible reagent for the selective synthesis of pyridine-containing heterocycles and metal-directed C–H functionalization. Its 4-methoxypyridine ligand enhances solubility and modulates redox behavior, while the bis(2,3-butanedione dioximate) framework enables controlled coordination chemistry. The system facilitates efficient cyclization reactions and functions effectively in transition-metal-catalyzed transformations requiring mild conditions and high functional group tolerance.

Safety Information

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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-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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