Methyl3-iodo-1-methyl-1H-indazole-6-carboxylate

97%

Reagent Code: #213353
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CAS Number 1041205-25-7

science Other reagents with same CAS 1041205-25-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.1 g/mol
Formula C₁₀H₉IN₂O₂
badge Registry Numbers
MDL Number MFCD15071434
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in research settings as an intermediate in the synthesis of bioactive compounds, this chemical serves as a building block in medicinal chemistry. It is particularly valuable in the development of novel pharmaceuticals targeting neurological and inflammatory pathways. Its structure allows for selective modifications, making it useful in structure-activity relationship (SAR) studies. Additionally, it has been employed in the preparation of analogs for cannabinoid receptor modulators, aiding in the exploration of endocannabinoid system functions. Due to its iodinated aromatic core, it also finds use in radiolabeling studies and imaging applications when tagged with radioactive isotopes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,080.00
inventory 250mg
10-20 days ฿5,070.00
inventory 1g
10-20 days ฿12,680.00
inventory 5g
10-20 days ฿36,980.00
inventory 10g
10-20 days ฿70,970.00
Methyl3-iodo-1-methyl-1H-indazole-6-carboxylate
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Used primarily in research settings as an intermediate in the synthesis of bioactive compounds, this chemical serves as a building block in medicinal chemistry. It is particularly valuable in the development of novel pharmaceuticals targeting neurological and inflammatory pathways. Its structure allows for selective modifications, making it useful in structure-activity relationship (SAR) studies. Additionally, it has been employed in the preparation of analogs for cannabinoid receptor modulators, aiding

Used primarily in research settings as an intermediate in the synthesis of bioactive compounds, this chemical serves as a building block in medicinal chemistry. It is particularly valuable in the development of novel pharmaceuticals targeting neurological and inflammatory pathways. Its structure allows for selective modifications, making it useful in structure-activity relationship (SAR) studies. Additionally, it has been employed in the preparation of analogs for cannabinoid receptor modulators, aiding in the exploration of endocannabinoid system functions. Due to its iodinated aromatic core, it also finds use in radiolabeling studies and imaging applications when tagged with radioactive isotopes.

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