(5'-BroMo-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-3-yl)-carbaMic acid tert-butyl ester

≥95%

Reagent Code: #149726
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CAS Number 1417793-65-7

science Other reagents with same CAS 1417793-65-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.26 g/mol
Formula C₁₅H₂₂BrN₃O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Commonly employed in research settings to design analogs with improved metabolic stability and binding affinity. Also utilized in solid-phase and combinatorial chemistry due to the presence of the tert-butyl carbamate (Boc) protecting group, which facilitates controlled deprotection and further functionalization.

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inventory 1g
10-20 days ฿41,290.00

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(5'-BroMo-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-3-yl)-carbaMic acid tert-butyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Commonly employed in research settings to design analogs with improved metabolic stability and binding affinity. Also utilized in solid-phase and combinatorial chemistry due to the presence of the tert-butyl carbamate (Boc) prot

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Commonly employed in research settings to design analogs with improved metabolic stability and binding affinity. Also utilized in solid-phase and combinatorial chemistry due to the presence of the tert-butyl carbamate (Boc) protecting group, which facilitates controlled deprotection and further functionalization.

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