2127-08-4 Usage
Heterocyclic compound
Two pyridine rings and a sulfur atom
The structure of 2-[(pyridin-4-ylmethyl)sulfanyl]pyridine is characterized by the presence of two pyridine rings (six-membered aromatic rings with one nitrogen atom) and a sulfur atom, making it a heterocyclic compound.
3. Unique structure and properties
The specific arrangement of the pyridine rings and the sulfur atom in 2-[(pyridin-4-ylmethyl)sulfanyl]pyridine contribute to its unique structure and properties, which may be of interest in pharmaceutical and chemical research.
Potential applications
Pharmaceutical and chemical research
Due to its unique structure and properties, 2-[(pyridin-4-ylmethyl)sulfanyl]pyridine may have potential applications in the fields of pharmaceutical and chemical research.
Coordination chemistry
Ligand
2-[(pyridin-4-ylmethyl)sulfanyl]pyridine may have the potential to act as a ligand in coordination chemistry, which involves the formation of complexes between metal ions and organic molecules.
Building block for synthesis
Complex organic compounds
The compound may also serve as a building block for the synthesis of other more complex organic compounds, further expanding its potential applications in various fields of chemistry and medicine.
Further research
Utility in chemistry and medicine
Additional research into the properties and potential uses of 2-[(pyridin-4-ylmethyl)sulfanyl]pyridine could uncover its utility in various fields of chemistry and medicine, potentially leading to new applications and discoveries.
Check Digit Verification of cas no
The CAS Registry Mumber 2127-08-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2127-08:
(6*2)+(5*1)+(4*2)+(3*7)+(2*0)+(1*8)=54
54 % 10 = 4
So 2127-08-4 is a valid CAS Registry Number.
2127-08-4Relevant articles and documents
Versatile C(sp2)?C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes
Dean, William M.,?iau?iulis, Mindaugas,Storr, Thomas E.,Lewis, William,Stockman, Robert A.
supporting information, p. 10013 - 10016 (2016/08/16)
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomerically pure diarylalkanes in up to 98 % yield and greater than 99.5 % enantiomeric excess. This ligand coupling reaction is tolerant to multiple substitution patterns and provides access to diverse areas of chemical space in three operationally simple steps from commercially available reagents. This strategy provides orthogonal access to electron-deficient heteroaromatic compounds, which are traditionally synthesized by transition metal catalyzed cross-couplings, and circumvents common issues associated with proto-demetalation and β-hydride elimination.
