(S)-Benzyl 2-methyl-3-oxopiperazine-1-carboxylate

95%

Reagent Code: #38330
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CAS Number 1373232-22-4

science Other reagents with same CAS 1373232-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.2777 g/mol
Formula C₁₃H₁₆N₂O₃
badge Registry Numbers
MDL Number MFCD22201137
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the production of various piperazine-based compounds, which are often explored for their potential therapeutic properties. Its structure is valuable in the design and creation of drug candidates targeting neurological disorders, such as anxiety, depression, and schizophrenia, due to the piperazine moiety's ability to interact with neurotransmitter receptors. Additionally, it is employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in achieving enantioselective synthesis. Its application extends to medicinal chemistry, where it aids in the optimization of drug-like properties, including bioavailability and metabolic stability.

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inventory 100mg
10-20 days ฿7,506.00

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(S)-Benzyl 2-methyl-3-oxopiperazine-1-carboxylate
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the production of various piperazine-based compounds, which are often explored for their potential therapeutic properties. Its structure is valuable in the design and creation of drug candidates targeting neurological disorders, such as anxiety, depression, and schizophrenia, due to the piperazine moiety's ability t

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the production of various piperazine-based compounds, which are often explored for their potential therapeutic properties. Its structure is valuable in the design and creation of drug candidates targeting neurological disorders, such as anxiety, depression, and schizophrenia, due to the piperazine moiety's ability to interact with neurotransmitter receptors. Additionally, it is employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in achieving enantioselective synthesis. Its application extends to medicinal chemistry, where it aids in the optimization of drug-like properties, including bioavailability and metabolic stability.

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