7-bromo-3-hydroxy-N-(2-methoxyphenyl)naphthalene-2-carboxamide

95%

Reagent Code: #219395
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CAS Number 1237-75-8

science Other reagents with same CAS 1237-75-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.22 g/mol
Formula C₁₈H₁₄O₃BrN
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors, particularly targeting protein kinases involved in inflammatory pathways and cancer progression. Its structural features allow for strong binding interactions with enzyme active sites, making it valuable in developing anti-inflammatory and anticancer agents. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when substituted on the naphthalene core. Additionally, it serves as a building block in the preparation of fluorescent probes for biochemical assays, leveraging its aromatic framework for detectable signaling in cellular environments.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,340.00
inventory 250mg
10-20 days ฿10,620.00
inventory 1g
10-20 days ฿28,850.00

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7-bromo-3-hydroxy-N-(2-methoxyphenyl)naphthalene-2-carboxamide
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Used in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors, particularly targeting protein kinases involved in inflammatory pathways and cancer progression. Its structural features allow for strong binding interactions with enzyme active sites, making it valuable in developing anti-inflammatory and anticancer agents. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when subs

Used in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors, particularly targeting protein kinases involved in inflammatory pathways and cancer progression. Its structural features allow for strong binding interactions with enzyme active sites, making it valuable in developing anti-inflammatory and anticancer agents. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when substituted on the naphthalene core. Additionally, it serves as a building block in the preparation of fluorescent probes for biochemical assays, leveraging its aromatic framework for detectable signaling in cellular environments.

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