6-(Hydroxymethyl)-2-methyl-2H-indazole

98%

Reagent Code: #196340
fingerprint
CAS Number 1159511-53-1

science Other reagents with same CAS 1159511-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.19 g/mol
Formula C₉H₁₀N₂O
badge Registry Numbers
MDL Number MFCD12028588
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anti-inflammatory and anticancer agents due to its structural similarity to purine bases, allowing interaction with enzyme active sites. Also employed in the preparation of novel indazole derivatives for structure-activity relationship (SAR) studies. Its hydroxymethyl group enables further functionalization, making it valuable in medicinal chemistry for creating diverse compound libraries.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,700.00
250mg
10-20 days ฿6,880.00
1g
10-20 days ฿16,220.00
6-(Hydroxymethyl)-2-methyl-2H-indazole
No image available

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anti-inflammatory and anticancer agents due to its structural similarity to purine bases, allowing interaction with enzyme active sites. Also employed in the preparation of novel indazole derivatives for structure-activity relationship (SAR) studies. Its hydroxymethyl group enables further functionalization, making it valuable in me

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anti-inflammatory and anticancer agents due to its structural similarity to purine bases, allowing interaction with enzyme active sites. Also employed in the preparation of novel indazole derivatives for structure-activity relationship (SAR) studies. Its hydroxymethyl group enables further functionalization, making it valuable in medicinal chemistry for creating diverse compound libraries.

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...