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(S)-1-ethylpyrrolidin-3-ylamine, with the molecular formula C7H15N, is a chemical compound characterized by an amine with a pyrrolidine ring structure and an ethyl group attached to the nitrogen atom. (S)-1-ethylpyrrolidin-3-ylamine is significant in the field of organic synthesis and pharmaceutical development due to its unique structural features and versatile applications.

216667-65-1

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216667-65-1 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-1-ethylpyrrolidin-3-ylamine is used as a chiral building block for the preparation of pharmaceuticals, contributing to the development of new drugs with improved efficacy and selectivity. Its unique structure allows for the creation of a wide range of enantiopure compounds, which are essential in the pharmaceutical industry to ensure the desired therapeutic effects and minimize potential side effects.
Used in Agrochemicals:
In the agrochemical industry, (S)-1-ethylpyrrolidin-3-ylamine serves as a chiral building block for the synthesis of various agrochemicals, such as pesticides and herbicides. Its use in this field helps in the development of more effective and environmentally friendly products by enhancing the selectivity and reducing the potential for harmful side effects on non-target organisms.
Used as a Chiral Auxiliary:
(S)-1-ethylpyrrolidin-3-ylamine is utilized as a chiral auxiliary in asymmetric synthesis, a crucial technique in organic chemistry that allows for the selective production of one enantiomer over the other. This selective synthesis is vital for creating enantiomerically pure compounds, which often exhibit different biological activities and are essential for the development of high-quality pharmaceuticals and other specialty chemicals.
Used as a Chiral Ligand:
Furthermore, (S)-1-ethylpyrrolidin-3-ylamine is employed as a chiral ligand in metal-catalyzed reactions, which are widely used in the synthesis of complex organic molecules. Its use as a chiral ligand enhances the selectivity and efficiency of these reactions, leading to the production of enantiomerically pure compounds with high yields and minimal side products.

Check Digit Verification of cas no

The CAS Registry Mumber 216667-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,6,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 216667-65:
(8*2)+(7*1)+(6*6)+(5*6)+(4*6)+(3*7)+(2*6)+(1*5)=151
151 % 10 = 1
So 216667-65-1 is a valid CAS Registry Number.

216667-65-1Relevant academic research and scientific papers

METHODS OF TREATING LIVER DISEASES

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Paragraph 00463, (2014/05/24)

The invention provides tricyclic compounds and their use in treating liver disorders, such as non-alcoholic steatohepatitis and related disorders (e.g., fibrosis). The compounds are contemplated to have activity against methionyl aminopeptidase 2.

PHENYL SULFONYL DERIVATIVES AND THEIR USE AS HISTAMINE H3 ANTAGONISTS

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, (2011/10/13)

A compound having the formula (1) wherein W represents N or CH; R1 represents H or C1-3 alkyl; R2 represents a N-containing heterocyclyl ring or a -C1-3 alkylene-N-containing heterocyclyl group; in which any N-c

TROPANE COMPOUNDS

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Page/Page column 377, (2009/05/30)

A compound according to Formula I or II: (I) or (II) wherein R1, R1b, R2, L1, and L2 and L2b are as defined in the specification, pharmaceutical compositions thereof, and methods of use thereof.

Structure-selectivity relationship in alkyllithium-aldehyde condensations using 3-aminopyrrolidine lithium amides as chiral auxiliaries

Corruble, Aline,Valnot, Jean-Yves,Maddaluno, Jacques,Duhamel, Pierre

, p. 8266 - 8275 (2007/10/03)

A nonracemizing route to a set of chiral 3-aminopyrrolidines, based on 4-hydroxy-(L)-proline, is described. The induction potential of the lithium amides derived from these diamines has then been investigated in the asymmetric addition of alkyllithium com

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