(S)-2,6-Diamino-N-(4-(5-fluorobenzo[d]thiazol-2-yl)-2-methylphenyl)hexanamide dihydrochloride

≥98%

Reagent Code: #233296
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CAS Number 328087-38-3

science Other reagents with same CAS 328087-38-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 459.41 g/mol
Formula C₂₀H₂₅Cl₂FN₄OS
badge Registry Numbers
MDL Number MFCD06407804
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of targeted cancer therapies due to its structural affinity for specific enzyme targets involved in cell signaling pathways. Also employed in the preparation of peptide-based molecules with enhanced metabolic stability and binding selectivity. Its fluorinated benzothiazole moiety contributes to improved pharmacokinetic properties, making it valuable in medicinal chemistry for optimizing drug candidates.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿4,940.00
inventory 5mg
10-20 days ฿15,830.00

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(S)-2,6-Diamino-N-(4-(5-fluorobenzo[d]thiazol-2-yl)-2-methylphenyl)hexanamide dihydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of targeted cancer therapies due to its structural affinity for specific enzyme targets involved in cell signaling pathways. Also employed in the preparation of peptide-based molecules with enhanced metabolic stability and binding selectivity. Its fluorinated benzothiazole moiety contributes to improved pharmacokinetic properties, maki

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of targeted cancer therapies due to its structural affinity for specific enzyme targets involved in cell signaling pathways. Also employed in the preparation of peptide-based molecules with enhanced metabolic stability and binding selectivity. Its fluorinated benzothiazole moiety contributes to improved pharmacokinetic properties, making it valuable in medicinal chemistry for optimizing drug candidates.

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