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2-((S)-2-Methoxymethyl-pyrrolidin-1-yl)-1-phenyl-propan-1-one is a complex organic compound with the molecular formula C16H21NO3. It is a chiral molecule, with the "S" configuration indicating that it is the levorotatory enantiomer. 2-((S)-2-Methoxymethyl-pyrrolidin-1-yl)-1-phenyl-propan-1-one is characterized by a propanone (ketone) group, a phenyl ring, and a pyrrolidine ring with a methoxymethyl group attached to it. The presence of the methoxymethyl group suggests potential applications in pharmaceuticals or as a synthetic intermediate due to its ability to act as a protecting group or a functional group in further chemical reactions. The specific arrangement of atoms and the chiral center in 2-((S)-2-Methoxymethyl-pyrrolidin-1-yl)-1-phenyl-propan-1-one can influence its reactivity, physical properties, and potential biological activity.

82215-90-5

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82215-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82215-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,1 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82215-90:
(7*8)+(6*2)+(5*2)+(4*1)+(3*5)+(2*9)+(1*0)=115
115 % 10 = 5
So 82215-90-5 is a valid CAS Registry Number.

82215-90-5Downstream Products

82215-90-5Relevant academic research and scientific papers

C-C - CONNECTIVE SYNTHESIS OF α-DIALKYLAMINO - KETONES FROM ALDEHYDES AND SEC.-AMINES

Enders, Dieter,Lotter, Hermann

, p. 639 - 642 (2007/10/02)

A simple and efficient 3 - step synthesis of α-dialkylamino - ketones 3 starting from aldehydes and sec.-amines is described.The unsymmetrically aminoketones are obtained as pure regioisomers via reaction of metalated α-aminonitriles 1 with aldehydes, followed by thermal HCN-elimination/tautomerization.

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