N-Hydroxy-4-methanesulfonylbenzene-1-carboximidamide

98%

Reagent Code: #220575
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CAS Number 56935-74-1

science Other reagents with same CAS 56935-74-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.24 g/mol
Formula C₈H₁₀N₂O₃S
badge Registry Numbers
MDL Number MFCD20486442
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a key building block in creating biologically active molecules due to its ability to form stable amide and amidine bonds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting inflammatory and oncological pathways. Its hydroxylated amidine structure enhances binding affinity to specific enzyme active sites, improving potency and selectivity.

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inventory 100mg
10-20 days ฿2,260.00

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N-Hydroxy-4-methanesulfonylbenzene-1-carboximidamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a key building block in creating biologically active molecules due to its ability to form stable amide and amidine bonds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting inflammatory and oncological pathways. Its hydroxylated amidine structure enhances bin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a key building block in creating biologically active molecules due to its ability to form stable amide and amidine bonds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting inflammatory and oncological pathways. Its hydroxylated amidine structure enhances binding affinity to specific enzyme active sites, improving potency and selectivity.

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