Date published: 2025-9-26

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(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) (CAS 176763-62-5)

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CAS Number:
176763-62-5
Molecular Weight:
603.74
Molecular Formula:
C36H52CoN2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) represents an intriguing organometallic compound featuring cobalt and a cyclohexane ring. As an organometallic complex, it forms a coordination compound with a metal atom and a carbon-based ligand. The versatile (R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) finds numerous applications in scientific research. Its capacity to bind to specific sites on enzymes has proven valuable in the study of enzymatic activity inhibition. Moreover, (R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) has been instrumental in exploring protein-protein interactions, forming stable complexes between two proteins. Additionally, its utility extends to the study of DNA and RNA, as it can bind to specific sites on these nucleic acids, resulting in activity inhibition. (R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) exerts its mechanism of action by selectively binding to specific sites on proteins, enzymes, DNA, and RNA, leading to the formation of stable complexes. This binding effectively inhibits the normal function of the targeted molecule, enabling detailed investigations into its structure, function, and interactions with other molecules.


(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) (CAS 176763-62-5) References

  1. Synthetic Strategy for Preparing Chiral Double-semicrystalline Polyether Block Copolymers.  |  McGrath, AJ., et al. 2015. Polym Chem. 6: 1465-1473. PMID: 25914726
  2. Aerobic Linear Allylic C-H Amination: Overcoming Benzoquinone Inhibition.  |  Pattillo, CC., et al. 2016. J Am Chem Soc. 138: 1265-72. PMID: 26730458
  3. Design, Synthesis, and Evaluation of Irciniastatin Analogues: Simplification of the Tetrahydropyran Core and the C(11) Substituents.  |  Liu, Q., et al. 2016. J Org Chem. 81: 1930-42. PMID: 26879056
  4. Synthetic Access to the Mandelalide Family of Macrolides: Development of an Anion Relay Chemistry Strategy.  |  Nguyen, MH., et al. 2018. J Org Chem. 83: 4287-4306. PMID: 29480727

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 1 g

sc-250835
1 g
$39.00

(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 5 g

sc-250835A
5 g
$126.00

(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 25 g

sc-250835B
25 g
$561.00

(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 100 g

sc-250835C
100 g
$1479.00

(R,R)-(−)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 1 kg

sc-250835D
1 kg
$6528.00