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N-methyl-N-(o-tolyl)propionamide is an organic compound with the chemical formula C11H15NO. It is a derivative of propionamide, featuring an N-methyl group and an o-tolyl group attached to the nitrogen atom. The o-tolyl group is a methyl-substituted phenyl ring, specifically at the ortho position (adjacent to the amide group). N-methyl-N-(o-tolyl)propionamide is a white crystalline solid and is used in various chemical syntheses, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure provides a balance of lipophilicity and hydrogen bonding capabilities, which can be crucial for its interaction with biological targets. The compound is also known for its potential applications in the development of new materials and as a building block in the synthesis of more complex molecules.

3558-09-6

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3558-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3558-09-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3558-09:
(6*3)+(5*5)+(4*5)+(3*8)+(2*0)+(1*9)=96
96 % 10 = 6
So 3558-09-6 is a valid CAS Registry Number.

3558-09-6Relevant academic research and scientific papers

Cross-Dehydrogenative Cyclization-Dimerization Cascade Sequence for the Synthesis of Symmetrical 3,3′-Bisoxindoles

Dobah, Farhaan,Mazodze, C. Munashe,Petersen, Wade F.

supporting information, p. 5466 - 5470 (2021/07/31)

The synthesis of symmetrical 3,3′-bisoxindoles from simple acyclic β-oxoanilides is reported. The described method forges three new C-C bonds in a single step via a sequential Mn(OAc)3·2H2O mediated oxidative radical cyclization-fragmentation-dimerization process. The scope of this reaction is demonstrated in the preparation of a variety of 3,3′-bisoxindoles, as well as its application toward the formal synthesis of the Calycanthaceae alkaloid, (±)-folicanthine.

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