(3aS,8aR)-2-(5-Bromopyridin-2-yl)-3a,8a-dihydro-8H-indeno[1,2-d]oxazole

97%, 99% e.e.

Reagent Code: #233440
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CAS Number 2757083-29-5

science Other reagents with same CAS 2757083-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.16 g/mol
Formula C₁₅H₁₁BrN₂O
thermostat Physical Properties
Boiling Point 443.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.67±0.1 g/cm3(Predicted)
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 structure enables strong binding to specific enzyme targets, enhancing potency in cell signaling pathway modulation. Commonly employed in pharmaceutical research for optimizing drug candidates targeting solid tumors. Also utilized in the preparation of neuroprotective compounds due to its ability to cross the blood-brain barrier in preclinical models.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,170.00
inventory 250mg
10-20 days ฿16,460.00
(3aS,8aR)-2-(5-Bromopyridin-2-yl)-3a,8a-dihydro-8H-indeno[1,2-d]oxazole
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Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of anticancer agents. Its structure enables strong binding to specific enzyme targets, enhancing potency in cell signaling pathway modulation. Commonly employed in pharmaceutical research for optimizing drug candidates targeting solid tumors. Also utilized in the preparation of neuroprotective compounds due to its ability to cross the blood-brain barrier in preclinical models.

Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of anticancer agents. Its structure enables strong binding to specific enzyme targets, enhancing potency in cell signaling pathway modulation. Commonly employed in pharmaceutical research for optimizing drug candidates targeting solid tumors. Also utilized in the preparation of neuroprotective compounds due to its ability to cross the blood-brain barrier in preclinical models.

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