N-methyl-1-(2-thiomorpholinopyridin-4-yl)methanamine

98%

Reagent Code: #216560
fingerprint
CAS Number 906352-66-7

science Other reagents with same CAS 906352-66-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.34 g/mol
Formula C₁₁H₁₇N₃S
badge Registry Numbers
MDL Number MFCD09702364
inventory_2 Storage & Handling
Storage Room temperature

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 treatments for inflammatory diseases and certain cancers due to its ability to modulate signaling pathways. Also employed in the design of selective receptor antagonists and enzyme inhibitors, making it valuable in drug discovery programs. Its structural features support improved binding affinity and metabolic stability in lead compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,790.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-methyl-1-(2-thiomorpholinopyridin-4-yl)methanamine
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 treatments for inflammatory diseases and certain cancers due to its ability to modulate signaling pathways. Also employed in the design of selective receptor antagonists and enzyme inhibitors, making it valuable in drug discovery programs. Its structural features support improved binding affinity and metabolic stability in lead comp

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of treatments for inflammatory diseases and certain cancers due to its ability to modulate signaling pathways. Also employed in the design of selective receptor antagonists and enzyme inhibitors, making it valuable in drug discovery programs. Its structural features support improved binding affinity and metabolic stability in lead compounds.

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...