(S)-4-(tert-Butyl)-2-(6-methylpyridin-2-yl)-4,5-dihydrooxazole

97%

Reagent Code: #38500
fingerprint
CAS Number 199277-80-0

science Other reagents with same CAS 199277-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.2900 g/mol
Formula C₁₃H₁₈N₂O
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is prominent in the pharmaceutical industry for the production of chiral intermediates, which are essential for synthesizing active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in academic and industrial research for developing novel catalytic processes and exploring new synthetic pathways. Its robust structure and ability to induce high stereoselectivity make it a valuable tool in organic chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,570.00
inventory 250mg
10-20 days ฿6,640.00
inventory 1g
10-20 days ฿21,990.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-4-(tert-Butyl)-2-(6-methylpyridin-2-yl)-4,5-dihydrooxazole
No image available

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is prominent in the pharmaceutical industry for the production of chiral intermediates, which are essential for synthesizing active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in academic and industrial

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is prominent in the pharmaceutical industry for the production of chiral intermediates, which are essential for synthesizing active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in academic and industrial research for developing novel catalytic processes and exploring new synthetic pathways. Its robust structure and ability to induce high stereoselectivity make it a valuable tool in organic chemistry.

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...