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6-(methylsulfanyl)pyridine-3-carboxamide is a chemical compound with the molecular formula C7H8N2OS. It is a derivative of pyridine, featuring a methylsulfanyl (-SCH3) group at the 6th position and a carboxamide (-CONH2) group at the 3rd position. 6-(methylsulfanyl)pyridine-3-carboxamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and drugs. Its structure provides a unique combination of sulfur and nitrogen-containing functional groups, which can contribute to its reactivity and utility in chemical transformations. The compound is typically synthesized through various chemical routes, and its properties, such as solubility and stability, can be influenced by the presence of these functional groups.

7151-91-9

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7151-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7151-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7151-91:
(6*7)+(5*1)+(4*5)+(3*1)+(2*9)+(1*1)=89
89 % 10 = 9
So 7151-91-9 is a valid CAS Registry Number.

7151-91-9Relevant academic research and scientific papers

Novel nicotinamide analog as inhibitor of nicotinamide N-methyltransferase

Ruf, Sven,Hallur, Mahanandeesha Siddappa,Anchan, Nisha K.,Swamy, Indu N.,Murugesan, Karthikai Raj,Sarkar, Sayantani,Narasimhulu, Lokesh Kananti,Putta, V.P. Rama Kishore,Shaik, Shama,Chandrasekar, Devaraj Venkatapura,Mane, Vishal Subhash,Kadnur, Sanjay Venkatachalapathi,Suresh, Juluri,Bhamidipati, Ravi Kanth,Singh, Manvi,Burri, Raghunadha Reddy,Kristam, Rajendra,Schreuder, Herman,Czech, Joerg,Rudolph, Christine,Marker, Alexander,Langer, Thomas,Mullangi, Ramesh,Yura, Takeshi,Gosu, Ramachandraiah,Kannt, Aimo,Dhakshinamoorthy, Saravanakumar,Rajagopal, Sridharan

supporting information, p. 922 - 925 (2018/02/14)

Nicotinamide N-methyltransferase (NNMT) has been linked to obesity and diabetes. We have identified a novel nicotinamide (NA) analog, compound 12 that inhibited NNMT enzymatic activity and reduced the formation of 1-methyl-nicotinamide (MNA), the primary metabolite of NA by ～80% at 2 h when dosed in mice orally at 50 mg/kg.

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