N-BOC-2-CYANOTHIOMORPHOLINE

97%

Reagent Code: #218706
fingerprint
CAS Number 1311254-50-8

science Other reagents with same CAS 1311254-50-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.31 g/mol
Formula C₁₀H₁₆N₂O₂S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure supports the development of kinase inhibitors and other targeted therapies. The BOC-protected amine allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. The thiomorpholine core with a nitrile group offers a versatile scaffold for medicinal chemistry optimization, including improving metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and anticancer agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,910.00
N-BOC-2-CYANOTHIOMORPHOLINE
No image available

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure supports the development of kinase inhibitors and other targeted therapies. The BOC-protected amine allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. The thiomorpholine core with a nitrile group offers a versatile scaffold for medicinal chemistry optimization, including improving metabolic stability and binding

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure supports the development of kinase inhibitors and other targeted therapies. The BOC-protected amine allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. The thiomorpholine core with a nitrile group offers a versatile scaffold for medicinal chemistry optimization, including improving metabolic stability and binding affinity. Commonly employed in the preparation of protease inhibitors and anticancer agents.

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...