2-Methyl-N-(1R-naphthalen-1-yl-ethyl)-5-nitrobenzamide

97%

Reagent Code: #213935
fingerprint
CAS Number 1093070-15-5

science Other reagents with same CAS 1093070-15-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.37 g/mol
Formula C₂₀H₁₈N₂O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules. Its structure supports development of selective enzyme inhibitors, particularly in studies targeting inflammatory pathways and cancer-related proteins. The nitro group allows further functionalization, enabling creation of diverse compound libraries for drug discovery. Also employed in asymmetric synthesis due to the chiral center, aiding in the production of enantiomerically pure drugs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,800.00
inventory 250mg
10-20 days ฿6,400.00
inventory 1g
10-20 days ฿12,790.00
inventory 5g
10-20 days ฿46,740.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Methyl-N-(1R-naphthalen-1-yl-ethyl)-5-nitrobenzamide
No image available

Used primarily in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules. Its structure supports development of selective enzyme inhibitors, particularly in studies targeting inflammatory pathways and cancer-related proteins. The nitro group allows further functionalization, enabling creation of diverse compound libraries for drug discovery. Also employed in asymmetric synthesis due to the chiral center, aiding in the production of enantiomerically pure drugs.

Used primarily in pharmaceutical research as a chiral intermediate for synthesizing bioactive molecules. Its structure supports development of selective enzyme inhibitors, particularly in studies targeting inflammatory pathways and cancer-related proteins. The nitro group allows further functionalization, enabling creation of diverse compound libraries for drug discovery. Also employed in asymmetric synthesis due to the chiral center, aiding in the production of enantiomerically pure drugs.

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...