(S)-2-tert-ButylcarboxaMide-4-tert-butoxycarbonylpiperazine

≥95%

Reagent Code: #46816
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CAS Number 150323-35-6

science Other reagents with same CAS 150323-35-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.38 g/mol
Formula C₁₄H₂₇N₃O₃
badge Registry Numbers
MDL Number MFCD02682987
thermostat Physical Properties
Melting Point 105-109 °C
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical synthesis industries as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butylcarboxamide and a tert-butoxycarbonyl (Boc) protecting group, makes it particularly valuable in peptide synthesis. The Boc group is often employed to protect amine functionalities during the stepwise construction of peptides, ensuring selective reactions and preventing unwanted side reactions. Additionally, the tert-butyl group enhances the compound's stability, making it suitable for use in complex organic syntheses. It is also explored in the development of small molecule drugs, particularly those targeting neurological and cardiovascular disorders, due to its potential to modulate biological pathways effectively.

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inventory 1g
10-20 days ฿21,888.00

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(S)-2-tert-ButylcarboxaMide-4-tert-butoxycarbonylpiperazine
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This compound is primarily utilized in the pharmaceutical and chemical synthesis industries as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butylcarboxamide and a tert-butoxycarbonyl (Boc) protecting group, makes it particularly valuable in peptide synthesis. The Boc group is often employed to protect amine functionalities during the stepwise construction of peptides, ensuring selective reactions and preventing unwanted sid

This compound is primarily utilized in the pharmaceutical and chemical synthesis industries as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butylcarboxamide and a tert-butoxycarbonyl (Boc) protecting group, makes it particularly valuable in peptide synthesis. The Boc group is often employed to protect amine functionalities during the stepwise construction of peptides, ensuring selective reactions and preventing unwanted side reactions. Additionally, the tert-butyl group enhances the compound's stability, making it suitable for use in complex organic syntheses. It is also explored in the development of small molecule drugs, particularly those targeting neurological and cardiovascular disorders, due to its potential to modulate biological pathways effectively.

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