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2-methyl-6-(3-nitrophenyl)pyridine is an organic compound characterized by a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. In this specific compound, the pyridine ring is substituted with a methyl group at the 2nd position and a 3-nitrophenyl group at the 6th position. The 3-nitrophenyl group itself is a benzene ring with a nitro group (-NO2) attached at the 3rd carbon position. 2-methyl-6-(3-nitrophenyl)pyridine is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly due to its unique structure that can participate in various chemical reactions. It is important to handle such compounds with care, as the nitro group can be reactive and may pose safety concerns.

4385-65-3

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4385-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4385-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4385-65:
(6*4)+(5*3)+(4*8)+(3*5)+(2*6)+(1*5)=103
103 % 10 = 3
So 4385-65-3 is a valid CAS Registry Number.

4385-65-3Downstream Products

4385-65-3Relevant academic research and scientific papers

Meta-Selective CAr-H Nitration of Arenes through a Ru3(CO)12-Catalyzed Ortho-Metalation Strategy

Fan, Zhoulong,Ni, Jiabin,Zhang, Ao

, p. 8470 - 8475 (2016)

The first example of transition metal-catalyzed meta-selective CAr-H nitration of arenes is described. With the use of Ru3(CO)12 as the catalyst and Cu(NO3)2·3H2O as the nitro source, a wide spectrum of arenes bearing diversified N-heterocycles or oximido as the directing groups were nitrated with meta-selectivity exclusively. Mechanism studies have demonstrated the formation of a new 18e-octahedral ruthenium species as a key ortho-CAr-H metalated intermediate, which may be responsible for the subsequent meta-selective electrophilic aromatic substitution (SEAr). Moreover, this approach provides a fast-track strategy for atom/step economical synthesis of many useful pharmaceutical molecules.

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