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2-Methyl-6-pentylpyridine is an organic compound characterized by a pyridine ring, which is a six-membered aromatic ring containing two nitrogen atoms. In this specific compound, the pyridine ring is substituted with a methyl group at the 2nd position and a pentyl group at the 6th position. The methyl group is a single carbon atom bonded to three hydrogen atoms, while the pentyl group consists of a five-carbon chain. This chemical structure gives 2-methyl-6-pentylpyridine unique properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. The compound's molecular formula is C12H19N, and it has a molecular weight of 177.29 g/mol.

5394-28-5

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5394-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5394-28-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5394-28:
(6*5)+(5*3)+(4*9)+(3*4)+(2*2)+(1*8)=105
105 % 10 = 5
So 5394-28-5 is a valid CAS Registry Number.

5394-28-5Downstream Products

5394-28-5Relevant academic research and scientific papers

NNN-Ruthenium Catalysts for the Synthesis of Pyridines, Quinolines, and Pyrroles by Acceptorless Dehydrogenative Condensation

Deng, Danfeng,Hu, Bowen,Yang, Min,Chen, Dafa

, p. 2386 - 2394 (2018/07/31)

The bidentate ruthenium complex (HO-C5H3N-CO-C5H3N-C5H4N)Ru(CO)2Cl2 (2) could transform to a tridentate product (HO-C5H3N-CO-C5H3N-C5H4N)Ru(CO)Cl2 (3), which further reacted with CH3ONa in the presence of PPh3 to convert to two complexes [(OC5H3N-CO-C5H3N-C5H4N)Ru(PPh3)2(CO)]Cl- (4) and [(OC5H3N-CO-C5H3N-C5H4N)Ru(PPh3)(CO)Cl] (5), via -OH deprotonation. The catalytic coupling cyclizations of secondary alcohols with amino alcohols were investigated, and complex 3 exhibited the highest activity. The coupling reactions proceeded in air with only 0.2 mol % catalyst loading and had a broad scope for the synthesis of pyridines, quinolones, and pyrroles.

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