(4-Amino-6-methylpyridin-3-yl)methanol

≥95%

Reagent Code: #137104
fingerprint
CAS Number 15742-82-2

science Other reagents with same CAS 15742-82-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.17 g/mol
Formula C₇H₁₀N₂O
badge Registry Numbers
MDL Number MFCD19204957
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting inflammatory diseases and oncology. Also utilized in the preparation of pyridine-based derivatives with potential antimicrobial and antiviral properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,570.00
inventory 100mg
10-20 days ฿3,330.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4-Amino-6-methylpyridin-3-yl)methanol
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting inflammatory diseases and oncology. Also utilized in the preparation of pyridine-based derivatives with potential antimicrobial and antiviral properties

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting inflammatory diseases and oncology. Also utilized in the preparation of pyridine-based derivatives with potential antimicrobial and antiviral properties.

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...