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4-(3S)-3-Pyrrolidinyl-morpholine is a heterocyclic chemical compound characterized by the presence of both a pyrrolidine and a morpholine ring. As a derivative of morpholine, it exhibits unique structural and chemical properties that make it a valuable intermediate in various applications.

216669-67-9

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216669-67-9 Usage

Uses

Used in Organic Synthesis:
4-(3S)-3-Pyrrolidinyl-morpholine is used as a building block in organic synthesis for the development of new compounds with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(3S)-3-Pyrrolidinyl-morpholine is utilized as a key intermediate in the synthesis of potential drug candidates. Its unique structure and properties contribute to the discovery of novel medicinal compounds with therapeutic potential.
Used in Materials Science:
4-(3S)-3-Pyrrolidinyl-morpholine may also find applications in materials science, where its distinct chemical structure and reactivity can be leveraged to create innovative materials with specific properties.
Used in Agrochemicals:
4-(3S)-3-Pyrrolidinyl-morpholine may also have uses in the agrochemical industry, where its unique characteristics can be employed to develop new agrochemical products with improved performance and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 216669-67-9 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 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 216669-67:
(8*2)+(7*1)+(6*6)+(5*6)+(4*6)+(3*9)+(2*6)+(1*7)=159
159 % 10 = 9
So 216669-67-9 is a valid CAS Registry Number.

216669-67-9Downstream Products

216669-67-9Relevant academic research and scientific papers

HTT MODULATORS FOR TREATING HUNTINGTON'S DISEASE

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Page/Page column 114-115, (2021/11/20)

Provided herein are certain compounds useful as HTT modulators. Such compound are useful in the treatment of Huntington's disease.

From a novel HTS hit to potent, selective, and orally bioavailable KDM5 inhibitors

Liang, Jun,Labadie, Sharada,Zhang, Birong,Ortwine, Daniel F.,Patel, Snahel,Vinogradova, Maia,Kiefer, James R.,Mauer, Till,Gehling, Victor S.,Harmange, Jean-Christophe,Cummings, Richard,Lai, Tommy,Liao, Jiangpeng,Zheng, Xiaoping,Liu, Yichin,Gustafson, Amy,Van der Porten, Erica,Mao, Weifeng,Liederer, Bianca M.,Deshmukh, Gauri,An, Le,Ran, Yingqing,Classon, Marie,Trojer, Patrick,Dragovich, Peter S.,Murray, Lesley

supporting information, p. 2974 - 2981 (2017/05/31)

A high-throughput screening (HTS) of the Genentech/Roche library identified a novel, uncharged scaffold as a KDM5A inhibitor. Lacking insight into the binding mode, initial attempts to improve inhibitor potency failed to improve potency, and synthesis of

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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