N-(4-Methanesulfonyl-2-nitrophenyl)-2H-1, 3-benzodioxol-5-amine

95%

Reagent Code: #219482
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CAS Number 852702-51-3

science Other reagents with same CAS 852702-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.32 g/mol
Formula C₁₄H₁₂N₂O₆S
badge Registry Numbers
MDL Number MFCD06679104
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design compounds with antitumor and anti-inflammatory activities. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when substituted.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,080.00
inventory 250mg
10-20 days ฿10,320.00
inventory 1g
10-20 days ฿34,160.00

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N-(4-Methanesulfonyl-2-nitrophenyl)-2H-1, 3-benzodioxol-5-amine
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design compounds with antitumor and anti-inflammatory activities. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when substituted.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design compounds with antitumor and anti-inflammatory activities. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when substituted.

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