1-(5-bromo-1-tosyl-1H-indol-3-yl)ethanone

95%

Reagent Code: #196444
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CAS Number 265111-01-1

science Other reagents with same CAS 265111-01-1

blur_circular Chemical Specifications

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Weight 392.27 g/mol
Formula C₁₇H₁₄BrNO₃S
badge Registry Numbers
MDL Number MFCD18433363
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating compounds with high biological activity. Commonly employed in research settings to develop potential antitumor and anti-inflammatory agents. Also utilized in the preparation of fluorescent probes for biochemical assays due to its favorable reactivity and stability in coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,560.00
inventory 250mg
10-20 days ฿19,270.00
inventory 1g
10-20 days ฿38,530.00

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1-(5-bromo-1-tosyl-1H-indol-3-yl)ethanone
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Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating compounds with high biological activity. Commonly employed in research settings to develop potential antitumor and anti-inflammatory agents. Also utilized in the preparation of fluorescent probes for biochemical assays due to its favorable reactivity and s
Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating compounds with high biological activity. Commonly employed in research settings to develop potential antitumor and anti-inflammatory agents. Also utilized in the preparation of fluorescent probes for biochemical assays due to its favorable reactivity and stability in coupling reactions.
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