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3-(piperidin-4-yl)indolin-2-one is a synthetic chemical compound with the molecular formula C14H16N2O. It features a piperidine ring and an indolin-2-one moiety, which contribute to its potential biological activities. 3-(piperidin-4-yl)indolin-2-one has garnered interest in the fields of medicinal chemistry and drug design due to its therapeutic potential for various diseases, including cancer and neurological disorders.

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72831-89-1 Usage

Uses

Used in Pharmaceutical Development:
3-(piperidin-4-yl)indolin-2-one is utilized as a promising candidate in the development of novel pharmaceutical agents. Its unique chemical structure positions it as a potential drug target for the treatment of various diseases, particularly those with unmet medical needs.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 3-(piperidin-4-yl)indolin-2-one serves as a valuable compound for studying its interactions with biological targets. This research can lead to a better understanding of its mechanisms of action and potential applications in therapeutic interventions.
Used in Drug Design:
3-(piperidin-4-yl)indolin-2-one is employed in drug design to create new molecules with improved pharmacological properties. Its structural features can be modified to enhance specificity, potency, and safety, making it a versatile building block for the development of innovative therapeutic agents.
Used in Cancer Therapy:
3-(piperidin-4-yl)indolin-2-one is used as a potential anticancer agent, given its interest in medicinal chemistry. It may be developed to target specific cancer-related pathways or to enhance the effectiveness of existing treatments, offering new hope for patients with cancer.
Used in Neurological Disorder Treatment:
3-(piperidin-4-yl)indolin-2-one is also considered for use in the treatment of neurological disorders. Its potential biological activities suggest that it could be a valuable asset in developing new therapies for conditions such as Alzheimer's, Parkinson's, or other neurodegenerative diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 72831-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,3 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72831-89:
(7*7)+(6*2)+(5*8)+(4*3)+(3*1)+(2*8)+(1*9)=141
141 % 10 = 1
So 72831-89-1 is a valid CAS Registry Number.

72831-89-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Piperidin-4-yl)indolin-2-one

1.2 Other means of identification

Product number -
Other names 3-piperidin-4-yl-1,3-dihydroindol-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72831-89-1 SDS

72831-89-1Downstream Products

72831-89-1Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND, APPLICATION THEREOF, AND COMPOSITION CONTAINING SAME

-

Paragraph 0755; 0758-0759, (2022/03/07)

A heterocyclic compound represented by formula XI, a pharmaceutically acceptable salt, a solvate, or a solvate of a pharmaceutically acceptable salt thereof, use thereof, and a composition containing the same. The compound is novel in structure and has good STAT5 inhibitory activity.

Synthesis of new bridged tetrahydro-β-carbolines and spiro-fused quinuclidines

Burm, Brigitte E.A,Gremmen, Christiaan,Wanner, Martin J,Koomen, Gerrit-Jan

, p. 2039 - 2049 (2007/10/03)

Two series of chemically related, conformationally restricted ring systems were synthesized. Bridged tetrahydro-β-carbolines, designed as selective 5-HT receptor ligands, were formed via Pictet-Spengler condensation of cyclic tryptamine precursors. Oxidation of the indole 2-position of the precursors followed by condensation with aldehydes produced spiro-cyclic quinuclidines, containing important muscarine receptor pharmacophores.

Antihypertensive 2H-indol-2-ones

-

, (2008/06/13)

Novel optically active isomers or racemates of 1,3-dihydro-3-{1-[2-(2,3-dihydro-1,4-benzodioxin-2-yl)-2-hydroxyethyl]-piperidin-4-yl}-2H-indol-2-ones of the formula STR1 wherein R1 is selected from the group consisting of hydrogen, chlorine, bromine, fluorine and alkoxy of 1 to 5 carbon atoms and R2 is selected from the group consisting of hydrogen and alkyl of 1 to 5 carbon atoms and their non-toxic, pharmaceutically acceptable acid addition salts having antihypertensive activity and a novel process and intermediates for their preparation.

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