1-Benzyl 4-(tert-butyl) (S)-2-methylpiperazine-1,4-dicarboxylate

98%

Reagent Code: #40212
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CAS Number 1163793-31-4

science Other reagents with same CAS 1163793-31-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.4101 g/mol
Formula C₁₈H₂₆N₂O₄
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a piperazine ring and ester groups, makes it a valuable building block for creating biologically active molecules. It is often employed in the preparation of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. The chiral center and protective groups allow for selective reactions, enabling the production of enantiomerically pure substances. This is crucial in drug discovery, where the stereochemistry of a molecule can significantly impact its efficacy and safety. Additionally, it may be used in the study of structure-activity relationships to optimize drug candidates. Its versatility and specificity make it a key component in the synthesis of complex organic molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,180.00
inventory 1g
10-20 days ฿5,590.00
inventory 5g
10-20 days ฿19,670.00
inventory 25g
10-20 days ฿72,340.00

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1-Benzyl 4-(tert-butyl) (S)-2-methylpiperazine-1,4-dicarboxylate
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a piperazine ring and ester groups, makes it a valuable building block for creating biologically active molecules. It is often employed in the preparation of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. The chiral center and protective groups allow for selective reactions, enabli

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a piperazine ring and ester groups, makes it a valuable building block for creating biologically active molecules. It is often employed in the preparation of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. The chiral center and protective groups allow for selective reactions, enabling the production of enantiomerically pure substances. This is crucial in drug discovery, where the stereochemistry of a molecule can significantly impact its efficacy and safety. Additionally, it may be used in the study of structure-activity relationships to optimize drug candidates. Its versatility and specificity make it a key component in the synthesis of complex organic molecules.

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