1374155-84-6 Usage
General Description
3,5-bis(1-imidazolyl)pyridine, also known as BIPY, is a chemical compound that belongs to the class of pyridine derivatives. It is a bidentate ligand that is commonly used in coordination chemistry and organometallic complexes. BIPY has been widely utilized as a ligand in catalysis, as it has the ability to stabilize metal ions and promote desired reactivity in the formation of various organic and inorganic compounds. 3,5-bis(1-imidazoly)pyridine has also shown potential in medicinal and pharmaceutical applications, with research suggesting its possible use in the development of new drugs and therapeutic agents. Its unique structure and versatile properties make BIPY a valuable compound in various fields of science and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1374155-84-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,1,5 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1374155-84:
(9*1)+(8*3)+(7*7)+(6*4)+(5*1)+(4*5)+(3*5)+(2*8)+(1*4)=166
166 % 10 = 6
So 1374155-84-6 is a valid CAS Registry Number.
1374155-84-6Relevant articles and documents
Suzuki-Miyaura C-C coupling reactions catalysed by a homogeneous and nanosilica supported palladium(ii) N-heterocyclic carbene complex derived from 3,5-di(1-imidazolyl)pyridine
Pahlevanneshan, Zari,Moghadam, Majid,Mirkhani, Valiollah,Tangestaninejad, Shahram,Mohammadpoor-Baltork, Iraj,Rezaei, Saghar
, p. 9729 - 9734 (2015)
A new palladium N-heterocyclic carbene complex using 3,5-di(1H-imidazol-1-yl)pyridine (1) as a precursor was prepared. The complex was immobilized on 3-chloropropylated nanosilica as a support and characterized by FT-IR spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy, energy dispersive X-ray analysis, transmission electron microscopy and elemental analysis. The prepared catalyst was used as a heterogeneous catalyst in the Suzuki-Miyaura coupling reactions of various aryl halides with phenylboronic acid and the corresponding biphenyls were being produced in a high yield. The catalyst was recyclable under aerobic conditions without significant loss of activity. Also, the catalytic activity of homogeneous catalyst was investigated.
