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2-(4-Amino-phenoxy)-1-piperidin-1-yl-ethanone is a complex organic compound with the molecular formula C13H18N2O2. It features a piperidine ring, an ethanone group, and a phenoxy group with an amino substituent at the para position. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is an intermediate in the production of certain drugs and may also be used in the development of new chemical entities with specific therapeutic properties. The compound's structure allows for various functional group transformations, making it a versatile building block in organic synthesis.

76870-14-9

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76870-14-9 Usage

Piperidine derivative

The compound belongs to the class of piperidine derivatives, which are organic compounds that contain a six-membered heterocyclic ring consisting of five carbon atoms and one nitrogen atom.

Piperidin-1-yl ethanone substituent

The compound has a specific functional group attached to it, which is a piperidin-1-yl ethanone substituent. This group is responsible for the compound's specific chemical properties and reactivity.

4-amino-phenoxy group

Another important part of the compound's structure is the 4-amino-phenoxy group, which is a phenolic ring with an amino group attached at the 4-position. This group contributes to the compound's potential pharmaceutical applications.

Potential pharmaceutical applications

2-(4-AMINO-PHENOXY)-1-PIPERIDIN-1-YL-ETHANONE may be used in the development of drugs targeting specific receptors or biological pathways. This is due to its unique chemical structure and the presence of functional groups that can interact with biological targets.

Dependence on further research and testing

The specific properties and potential uses of this chemical compound would depend on further research and testing. This is because the compound's biological activity, pharmacokinetics, and safety profile need to be thoroughly investigated before it can be considered for pharmaceutical applications.

Significance in medicinal chemistry and drug development

The compound has potential significance in the field of medicinal chemistry and drug development due to its unique structure and potential pharmaceutical applications. Further research on 2-(4-AMINO-PHENOXY)-1-PIPERIDIN-1-YL-ETHANONE could lead to the discovery of new drugs targeting specific receptors or biological pathways, contributing to the advancement of medical treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 76870-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76870-14:
(7*7)+(6*6)+(5*8)+(4*7)+(3*0)+(2*1)+(1*4)=159
159 % 10 = 9
So 76870-14-9 is a valid CAS Registry Number.

76870-14-9Relevant academic research and scientific papers

(E)-3-(Aryl(arylamino)methylene)indolin-2-one derivatives: An efficient synthetic approach and evaluation of their cancer inhibitory activity

Jiang, Hongwu,Feng, Zhiyuan,Chen, Taiping,Li, Zicheng,Huang, Wencai,Luo, Youfu,Zhao, Yinglan

, p. 44 - 49 (2018/02/28)

A series of (E)-3-(aryl(arylamino)methylene)indolin-2-one derivatives were synthesised using an efficient synthetic approach. The method involved reaction of 3-bromo-3-(bromo(aryl)methyl)indolin-2-one with substituted anilines through nucleophilic substitution and a simultaneous elimination using NaHCO3 in DMF. The anticancer activity of the products against four cell lines, HCT-116, A549, SKOV3 and MDA-MB-231, was also evaluated, and several compounds showed moderate inhibitory activity.

Synthesis of Some New 3-Methoxy-4-acylaminophenylisothiocyanates, 4'-Isothiocyanatophenoxyacetamides/Isobutyramides as Possible Anthelmintic Agents

Shridhar, D. R.,Rao, K. Srinivasa,Singh, A. N.,Rastogi, K.,Jain, M. L.

, p. 1277 - 1280 (2007/10/02)

A number of new 3-methoxy-4-acylaminophenylisothiocyanates (II and III), 4'-isothiocyanatophenoxyacetamides (IV) and 4-isothiocyanatophenoxyisobutyramides (V) have been synthesized and tested for anthelmintic, antiamoebic and antitrichomonal activities.

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