(5aR,10bS)-9-Bromo-2-mesityl-4,5a,6,10b-tetrahydroindeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-2-ium tetrafluoroborate

97%

Reagent Code: #229578
label
Alias (5aR,10bS)-9-bromo-2-homotrimethyl-4,5a,6,10b-tetrahydroindeno[2,1-b][1,2,4]triazole[4,3-d][1,4]oxazine-2-onium tetrafluoroborate
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CAS Number 1644388-09-9

science Other reagents with same CAS 1644388-09-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 498.12 g/mol
Formula C₂₁H₂₁BBrF₄N₃O
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of anticancer agents. Its bromo and mesityl functional groups allow for further cross-coupling reactions, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for scaffold diversification and structure-activity relationship studies. Also utilized in the preparation of fluorescent probes due to its rigid polycyclic framework, which supports stable optical properties in imaging applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿45,130.00
250mg
10-20 days ฿68,820.00
1g
10-20 days ฿160,360.00
(5aR,10bS)-9-Bromo-2-mesityl-4,5a,6,10b-tetrahydroindeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-2-ium tetrafluoroborate
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Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of anticancer agents. Its bromo and mesityl functional groups allow for further cross-coupling reactions, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for scaffold diversification and structure-activity relationship studies. Also utilized in the preparation of fluorescent probes due to its rigid polycyclic framework

Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of anticancer agents. Its bromo and mesityl functional groups allow for further cross-coupling reactions, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for scaffold diversification and structure-activity relationship studies. Also utilized in the preparation of fluorescent probes due to its rigid polycyclic framework, which supports stable optical properties in imaging applications.

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