(S)-2-(6-Benzhydrylpyridin-2-yl)-4-cyclohexyl-4,5-dihydrooxazole

97%

Reagent Code: #237480
fingerprint
CAS Number 2640520-02-9

science Other reagents with same CAS 2640520-02-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 396.52 g/mol
Formula C₂₇H₂₈N₂O
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used in pharmaceutical research as a chiral intermediate for the synthesis of central nervous system (CNS) active compounds. Its structural features make it suitable for developing agents targeting neurological disorders, particularly those involving receptor modulation such as dopamine or serotonin receptors. The compound’s stereochemistry and rigid framework enhance selectivity and binding affinity in drug candidates. It is also employed in asymmetric synthesis and catalysis due to its oxazoline core, supporting the development of enantiomerically pure therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,350.00
inventory 250mg
10-20 days ฿19,300.00
inventory 1g
10-20 days ฿56,420.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-2-(6-Benzhydrylpyridin-2-yl)-4-cyclohexyl-4,5-dihydrooxazole
No image available

Used in pharmaceutical research as a chiral intermediate for the synthesis of central nervous system (CNS) active compounds. Its structural features make it suitable for developing agents targeting neurological disorders, particularly those involving receptor modulation such as dopamine or serotonin receptors. The compound’s stereochemistry and rigid framework enhance selectivity and binding affinity in drug candidates. It is also employed in asymmetric synthesis and catalysis due to its oxazoline core,

Used in pharmaceutical research as a chiral intermediate for the synthesis of central nervous system (CNS) active compounds. Its structural features make it suitable for developing agents targeting neurological disorders, particularly those involving receptor modulation such as dopamine or serotonin receptors. The compound’s stereochemistry and rigid framework enhance selectivity and binding affinity in drug candidates. It is also employed in asymmetric synthesis and catalysis due to its oxazoline core, supporting the development of enantiomerically pure therapeutics.

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...