6-Iodo-2-methyl-2H-indazole

98%

Reagent Code: #201152
fingerprint
CAS Number 1216387-68-6

science Other reagents with same CAS 1216387-68-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.06 g/mol
Formula C₈H₇IN₂
badge Registry Numbers
MDL Number MFCD11977524
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive iodine moiety, enabling coupling reactions such as Suzuki or Heck reactions to introduce aromatic or heteroaromatic groups. Its structure supports the design of biologically active molecules targeting neurological disorders and inflammatory diseases. Also employed in research settings for labeling and tracer studies owing to the presence of iodine, facilitating detection and imaging applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,610.00
inventory 250mg
10-20 days ฿10,990.00
inventory 1g
10-20 days ฿12,160.00
inventory 5g
10-20 days ฿38,140.00
6-Iodo-2-methyl-2H-indazole
No image available

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive iodine moiety, enabling coupling reactions such as Suzuki or Heck reactions to introduce aromatic or heteroaromatic groups. Its structure supports the design of biologically active molecules targeting neurological disorders and inflammatory diseases. Also employed in research s

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive iodine moiety, enabling coupling reactions such as Suzuki or Heck reactions to introduce aromatic or heteroaromatic groups. Its structure supports the design of biologically active molecules targeting neurological disorders and inflammatory diseases. Also employed in research settings for labeling and tracer studies owing to the presence of iodine, facilitating detection and imaging applications.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...