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1-(2-Aminoethyl)pyridin-2(1H)-one, also known as 2-AEPY, is a heterocyclic chemical compound with the molecular formula C7H9N3O. It features a pyridine ring and a primary amine functional group, making it a versatile compound with potential applications in pharmaceuticals, organic synthesis, and coordination chemistry.

35597-92-3

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35597-92-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-Aminoethyl)pyridin-2(1H)-one is used as a building block for organic synthesis, contributing to the development of new pharmaceutical compounds due to its unique structure and functional groups.
Used in Anti-inflammatory Applications:
1-(2-Aminoethyl)pyridin-2(1H)-one is used as an anti-inflammatory agent, potentially modulating inflammatory pathways and providing therapeutic benefits in treating inflammatory conditions.
Used in Anti-tumor Applications:
1-(2-Aminoethyl)pyridin-2(1H)-one is used as an anti-tumor agent, exhibiting potential to inhibit tumor growth and progression, making it a candidate for further research in oncology.
Used in Coordination Chemistry:
1-(2-Aminoethyl)pyridin-2(1H)-one is used as a ligand in coordination chemistry, leveraging its ability to chelate metal ions for various applications, including the development of catalysts and sensors.
Used in Metal Chelation:
1-(2-Aminoethyl)pyridin-2(1H)-one is used for its metal chelating properties, which can be beneficial in various industrial processes and environmental applications, such as the removal of heavy metals from wastewater.

Check Digit Verification of cas no

The CAS Registry Mumber 35597-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35597-92:
(7*3)+(6*5)+(5*5)+(4*9)+(3*7)+(2*9)+(1*2)=153
153 % 10 = 3
So 35597-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O/c8-4-6-9-5-2-1-3-7(9)10/h1-3,5H,4,6,8H2

35597-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-aminoethyl)pyridin-2-one

1.2 Other means of identification

Product number -
Other names 2'-TRIFLUOROMETHYLBIPHENYL-4-CARBALDEHYDE

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:35597-92-3 SDS

35597-92-3Downstream Products

35597-92-3Relevant academic research and scientific papers

TRI-CYCLE COMPOUND AND APPLICATIONS THEREOF

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Paragraph 0278-0279; 0281, (2020/01/22)

Disclosed in the present invention are a compound represented by formula (I), a tautomer thereof or a pharmaceutically acceptable salt, and applications thereof in the preparation of drugs for treating HBV-related diseases.

Photoreactive Derivative of Hyaluronic Acid, Method of Preparation Thereof, 3D.Crosslinked Derivative of Hyaluronic Acid, Method of Preparation and Use Thereof

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, (2015/11/16)

The subject-matter of the invention is a photoreactive derivative of hyaluronic acid (formula I) and the method of preparation thereof, where first an aldehyde derivative of hyaluronic acid is prepared, oxidized in the position 6 of the glucosamine cycle and then the oxidized derivative reacts with an amine carrying a photoreactive species, for example 1-(2-aminoethyl)pyridine-2(1H)-one, in the presence of a reducing agent, forming a photoreactive derivative. The prepared photoreactive derivative may be then photocrosslinked, wherein the reaction is based on [4+4] photocycloaddition. Moreover, the invention relates to a 3D-crosslinked derivative of hyaluronic acid (formula II) which exhibits an increased hydrolytic stability and improved sorption properties, with the possibility of a further design of the physical properties thereof according to the requirements of the final applications, and moreover, to the use thereof in tissue engineering, regenerative medicine, medical agents or formulations or cosmetics.

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