Methyl 4-methyl-7-nitro-1H-indole-2-carboxylate

≥95%

Reagent Code: #209022
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CAS Number 1956355-82-0

science Other reagents with same CAS 1956355-82-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.21 g/mol
Formula C₁₁H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD27922872
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective kinase inhibitors. Its structure supports activity in cell signaling research, especially in studies related to inflammation and cancer pathways. The nitro group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies. Commonly employed in medicinal chemistry for building indole-based scaffolds with biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿680.00
inventory 250mg
10-20 days ฿1,660.00
inventory 1g
10-20 days ฿6,540.00
inventory 5g
10-20 days ฿28,300.00

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Methyl 4-methyl-7-nitro-1H-indole-2-carboxylate
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective kinase inhibitors. Its structure supports activity in cell signaling research, especially in studies related to inflammation and cancer pathways. The nitro group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies. Commonly employed in medicinal chemistry for building indole-based scaffolds with biological a

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective kinase inhibitors. Its structure supports activity in cell signaling research, especially in studies related to inflammation and cancer pathways. The nitro group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies. Commonly employed in medicinal chemistry for building indole-based scaffolds with biological activity.

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