Tert-butyl 6-methoxy-3-methyl-1H-indazole-1-carboxylate

≥95%

Reagent Code: #240140
fingerprint
CAS Number 691900-70-6

science Other reagents with same CAS 691900-70-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.30 g/mol
Formula C₁₄H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD07780794
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports selective binding to enzyme active sites, enhancing drug efficacy. Commonly employed in medicinal chemistry for constructing indazole-based bioactive molecules. Also utilized in research settings to develop new therapeutic agents targeting inflammatory diseases and neurological disorders. Stable under standard storage conditions, making it suitable for multi-step organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,650.00
inventory 250mg
10-20 days ฿7,900.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tert-butyl 6-methoxy-3-methyl-1H-indazole-1-carboxylate
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports selective binding to enzyme active sites, enhancing drug efficacy. Commonly employed in medicinal chemistry for constructing indazole-based bioactive molecules. Also utilized in research settings to develop new therapeutic agents targeting inflammatory diseases and neurological disorders. Stable under standard storage conditions, making it

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports selective binding to enzyme active sites, enhancing drug efficacy. Commonly employed in medicinal chemistry for constructing indazole-based bioactive molecules. Also utilized in research settings to develop new therapeutic agents targeting inflammatory diseases and neurological disorders. Stable under standard storage conditions, making it suitable for multi-step organic syntheses.

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...