(R)-4-(tert-Butyl)-2-(6-phenylpyridin-2-yl)-4,5-dihydrooxazole

98% 99%ee

Reagent Code: #231394
fingerprint
CAS Number 2757082-75-8

science Other reagents with same CAS 2757082-75-8

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its oxazoline core with a stereogenic center enables selective binding to enzyme targets, enhancing drug potency and reducing off-target effects. Commonly employed in oncology drug research due to its ability to modulate signaling pathways involved in cell proliferation. Also utilized in asymmetric catalysis for the preparation of enantiomerically pure compounds in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,850.00
inventory 250mg
10-20 days ฿7,050.00
inventory 1g
10-20 days ฿21,880.00

Cart

No products

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

Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its oxazoline core with a stereogenic center enables selective binding to enzyme targets, enhancing drug potency and reducing off-target effects. Commonly employed in oncology drug research due to its ability to modulate signaling pathways involved in cell proliferation. Also utilized in asymmetric catalysis for the preparation of enantiomerically pure compounds in medicinal chem

Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its oxazoline core with a stereogenic center enables selective binding to enzyme targets, enhancing drug potency and reducing off-target effects. Commonly employed in oncology drug research due to its ability to modulate signaling pathways involved in cell proliferation. Also utilized in asymmetric catalysis for the preparation of enantiomerically pure compounds in medicinal 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...