(R)-4-Isobutyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole

97%

Reagent Code: #232165
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CAS Number 2757085-19-9

science Other reagents with same CAS 2757085-19-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.29 g/mol
Formula C₁₃H₁₈N₂O
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen. Its oxazoline core provides stereochemical control during catalytic reactions, making it valuable in asymmetric synthesis. It also serves as a ligand in transition metal-catalyzed reactions, enhancing enantioselectivity in hydrogenation and coupling processes. Additionally, it is employed in the development of optically active agrochemicals and fine chemicals where high enantiomeric purity is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,490.00
250mg
10-20 days ฿7,410.00
1g
10-20 days ฿29,010.00
(R)-4-Isobutyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole
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Used as a chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen. Its oxazoline core provides stereochemical control during catalytic reactions, making it valuable in asymmetric synthesis. It also serves as a ligand in transition metal-catalyzed reactions, enhancing enantioselectivity in hydrogenation and coupling processes. Additionally, it is employed in the development of optically activ

Used as a chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen. Its oxazoline core provides stereochemical control during catalytic reactions, making it valuable in asymmetric synthesis. It also serves as a ligand in transition metal-catalyzed reactions, enhancing enantioselectivity in hydrogenation and coupling processes. Additionally, it is employed in the development of optically active agrochemicals and fine chemicals where high enantiomeric purity is required.

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