Product Name:tert-Butyl 2-(2-oxopiperazin-1-yl)acetate

IUPAC Name:tert-butyl 2-(2-oxopiperazin-1-yl)acetate

CAS:176371-67-8
Molecular Formula:C10H18N2O3
Purity:95%+
Catalog Number:CM335170
Molecular Weight:214.26

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For R&D use only.

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Product Details

CAS NO:176371-67-8
Molecular Formula:C10H18N2O3
Melting Point:-
Smiles Code:O=C(OC(C)(C)C)CN1C(CNCC1)=O
Density:
Catalog Number:CM335170
Molecular Weight:214.26
Boiling Point:
MDL No:
Storage:2-8°C

Category Infos

Piperazines
Piperazine is an organic compound consisting of a six-membered ring containing two nitrogen atoms in opposite positions in the ring. The chemical formula of piperazine is C4H10N2, and it is an important pharmaceutical intermediate. Pyrimidines and piperazines are known to be the backbone of many bulk compounds and important core structures for approved drugs; studies have shown that combining a pyridine ring with a piperazine moiety within a single structural framework enhances biological activity.

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Product Other Information

Product Overview Tert-butyl 2-(2-oxopiperazin-1-yl)acetate, also known as TBOPA, is a small organic molecule with a wide range of applications in both research and industry. TBOPA has been used in a variety of research fields, including biochemistry, organic chemistry, and pharmacology. 
Synthesis Method Tert-butyl 2-(2-oxopiperazin-1-yl)acetate can be synthesized using a variety of methods, including the Wittig reaction, the Horner-Wittig reaction, and the Stork reaction. In the Wittig reaction, an aldehyde or ketone is reacted with a phosphonium salt to form an alkylidene, which is then reacted with an aldehyde or ketone to form an alkene. The Horner-Wittig reaction is a variant of the Wittig reaction, in which an aldehyde or ketone is reacted with a phosphonium salt to form an alkylidene, which is then reacted with an aldehyde or ketone to form a cyclic alkene. The Stork reaction is a variant of the Wittig reaction, in which an aldehyde or ketone is reacted with a phosphonium salt to form an alkylidene, which is then reacted with an aldehyde or ketone to form an alkylidene.
Chemical Properties Tert-butyl 2-(2-oxopiperazin-1-yl)acetate is relatively inexpensive and easy to obtain, and can be used in a variety of reactions and processes. In addition, it is relatively stable and can be stored for extended periods of time. Tert-butyl 2-(2-oxopiperazin-1-yl)acetate is a relatively small molecule, and can be difficult to handle in the laboratory. It is not very soluble in water, and can be difficult to dissolve in aqueous solutions.
Synthesis and Application Tert-butyl 2-(2-oxopiperazin-1-yl)acetate has been used in a variety of scientific research applications. Tert-butyl 2-(2-oxopiperazin-1-yl)acetate has been used as a reagent in organic synthesis, as a catalyst in chemical reactions, and as a substrate in biochemical and physiological studies. Tert-butyl 2-(2-oxopiperazin-1-yl)acetate has also been used to synthesize a variety of compounds, including drugs and other small molecules. In addition, Tert-butyl 2-(2-oxopiperazin-1-yl)acetate has been used in the study of biochemical and physiological processes, as well as in the development of new drugs and therapies.
Future Directions Tert-butyl 2-(2-oxopiperazin-1-yl)acetate could be used in the synthesis of a variety of compounds, including drugs, and could also be used as a catalyst or reagent in chemical reactions. Tert-butyl 2-(2-oxopiperazin-1-yl)acetate could also be used in the study of biochemical and physiological processes, as well as in the development of new drugs and therapies. In addition, Tert-butyl 2-(2-oxopiperazin-1-yl)acetate could be used in the development of new materials and technologies, such as nanomaterials and biosensors.