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N-benzyl-trans-3,4-dimethylpyrrolidine is an organic compound with the molecular formula C13H19N. It is a derivative of pyrrolidine, a heterocyclic amine with a four-membered ring containing one nitrogen atom. The compound features a benzyl group (C6H5CH2-) attached to the nitrogen atom, and two methyl groups (CH3-) at the 3rd and 4th positions of the pyrrolidine ring. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as its role as an intermediate in various chemical reactions. Due to its unique structure, N-benzyl-trans-3,4-dimethylpyrrolidine exhibits specific chemical properties and reactivity, making it a valuable compound in the field of organic chemistry.

4209-74-9

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4209-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4209-74-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4209-74:
(6*4)+(5*2)+(4*0)+(3*9)+(2*7)+(1*4)=79
79 % 10 = 9
So 4209-74-9 is a valid CAS Registry Number.

4209-74-9Downstream Products

4209-74-9Relevant academic research and scientific papers

Asymmetric desymmetrization of meso-pyrrolidine derivatives by enantiotopic selective C-H hydroxylation using (salen)manganese(III) complexes

Punniyamurthy,Katsuki, Tsutomu

, p. 9439 - 9454 (2007/10/03)

Chiral (salen)manganese(III) complexes 1 catalyzed the asymmetric desymmetrization of N-protected meso-pyrrolidine derivatives 3, 6-8, 15 and 18 by enantiotopic selective C-H oxidation in the presence of terminal oxidant iodosylbenzene. The oxidation occurred chemoselectively at the carbon α to the nitrogen atom to afford optically active hydroxypyrrolidine derivatives 9, 11, 13, 16, 19 and 21 that were further oxidized to chiral lactams with Jones reagent. The N-protecting groups of the meso-pyrrolidine derivatives have notable effect on the enantioselectivity.

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