N-piperidine Ibrutinib

≥97%

Reagent Code: #219288
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CAS Number 330785-90-5

science Other reagents with same CAS 330785-90-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.45 g/mol
Formula C₂₂H₂₂N₆O
inventory_2 Storage & Handling
Storage -20℃

description Product Description

N-piperidine Ibrutinib is a key synthetic intermediate used in the production of Ibrutinib, a targeted therapy for B-cell malignancies such as mantle cell lymphoma, chronic lymphocytic leukemia, and Waldenström's macroglobulinemia. This compound features a piperidine ring attached to the core pyrazolo[3,4-d]pyrimidine scaffold of Ibrutinib. In the final synthesis step, the piperidine nitrogen is acylated with an acryloyl group to form the active BTK inhibitor. As an intermediate, it plays a crucial role in enabling the selective inhibition of Bruton's tyrosine kinase (BTK) in the complete drug molecule, supporting the treatment of hematologic cancers.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿43,720.00
inventory 10mg
10-20 days ฿65,560.00
inventory 25mg
10-20 days ฿111,430.00

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N-piperidine Ibrutinib
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N-piperidine Ibrutinib is a key synthetic intermediate used in the production of Ibrutinib, a targeted therapy for B-cell malignancies such as mantle cell lymphoma, chronic lymphocytic leukemia, and Waldenström's macroglobulinemia. This compound features a piperidine ring attached to the core pyrazolo[3,4-d]pyrimidine scaffold of Ibrutinib. In the final synthesis step, the piperidine nitrogen is acylated with an acryloyl group to form the active BTK inhibitor. As an intermediate, it plays a crucial

N-piperidine Ibrutinib is a key synthetic intermediate used in the production of Ibrutinib, a targeted therapy for B-cell malignancies such as mantle cell lymphoma, chronic lymphocytic leukemia, and Waldenström's macroglobulinemia. This compound features a piperidine ring attached to the core pyrazolo[3,4-d]pyrimidine scaffold of Ibrutinib. In the final synthesis step, the piperidine nitrogen is acylated with an acryloyl group to form the active BTK inhibitor. As an intermediate, it plays a crucial role in enabling the selective inhibition of Bruton's tyrosine kinase (BTK) in the complete drug molecule, supporting the treatment of hematologic cancers.

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