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2-Oxo-1-piperazineacetic acid is an organic chemical compound that belongs to the class of piperazines, which are compounds featuring a six-membered piperazine ring with two nitrogen atoms and four carbon atoms. 2-Oxo-1-piperazineacetic acid is characterized by the presence of a carboxylic acid and a 2-oxo functional group, which together contribute to its basic and acidic properties. Although less commonly known and not extensively studied, 2-Oxo-1-piperazineacetic acid exhibits complex reactivity due to its functional groups, making it a candidate for various potential reactions and synthesis processes.

24860-46-6

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24860-46-6 Usage

Uses

Used in Pharmaceutical Industry:
2-Oxo-1-piperazineacetic acid is used as a building block for the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. The presence of both carboxylic and 2-oxo groups allows for a wide range of potential reactions, making it a versatile starting material for the development of new drugs.
Used in Chemical Research:
2-Oxo-1-piperazineacetic acid is used as a research compound in the field of organic chemistry, particularly for studying the reactivity and properties of carboxylic acids and 2-oxo compounds. Its complex reactivity and the presence of nitrogen in its structure make it an interesting subject for exploring new synthetic pathways and understanding the behavior of similar compounds.
Used in Material Science:
2-Oxo-1-piperazineacetic acid is used as a precursor in the development of new materials, such as polymers and composites, that can benefit from the unique properties of the compound. The carboxylic and 2-oxo groups can be utilized to create novel structures with enhanced properties, such as improved strength, flexibility, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 24860-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24860-46:
(7*2)+(6*4)+(5*8)+(4*6)+(3*0)+(2*4)+(1*6)=116
116 % 10 = 6
So 24860-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O3/c9-5-3-7-1-2-8(5)4-6(10)11/h7H,1-4H2,(H,10,11)

24860-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-oxopiperazin-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 1-Piperazineaceticacid,2-oxo

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:24860-46-6 SDS

24860-46-6Relevant academic research and scientific papers

Design, synthesis, and structure-activity relationships of unsubstituted piperazinone-based transition state factor Xa inhibitors

Huang, Wenrong,Naughton, Mary Ann,Yang, Hua,Su, Ting,Dam, Suiko,Wong, Paul W.,Arfsten, Ann,Edwards, Susan,Sinha, Uma,Hollenbach, Stanley,Scarborough, Robert M.,Zhu, Bing-Yan

, p. 723 - 728 (2007/10/03)

A series of novel transition state factor Xa inhibitors containing a variety of lactam ring systems as central templates was synthesized in an expedient manner and allowed for a great deal of structural variability. Among them, the piperazinone-based inhibitors were found to be not only active against factor Xa but also selective over thrombin. Optimization of the P4 moiety yielded several potent compounds with IC50 below 1 nM against factor Xa.

Complexes possessing ortho ligating functionality

-

, (2008/06/13)

A group of functionalized amine chelants having ortho ligating functionality that form complexes with rare-earth type metal ions are disclosed. The chelants possess the general formula STR1 wherein R'1, R'2, R'3, R'4, R'5 and R'6, Z' and X are all defined in the specification. In addition certain of the chelant-radionuclide complexes can be effectively employed in compositions useful as therapeutic and/or diagnostic agents for calcific tumors and/or relief of bone pain.

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