(R)-4-Isopropyl-2-(pyrimidin-2-yl)-4,5-dihydrooxazole

98% 99%ee

Reagent Code: #231390
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CAS Number 2757082-66-7

science Other reagents with same CAS 2757082-66-7

blur_circular Chemical Specifications

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

description Product Description

Used in pharmaceutical synthesis as a chiral intermediate, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Its oxazoline core acts as a directing group in asymmetric catalysis, enabling selective carbon–carbon bond formation. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic peptide structures and enhance metabolic stability. Also utilized in agrochemicals for creating enantioselective herbicides and fungicides. Its pyrimidine moiety allows for hydrogen bonding interactions, improving target binding affinity in drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,250.00
inventory 250mg
10-20 days ฿5,810.00
inventory 1g
10-20 days ฿21,580.00
inventory 5g
10-20 days ฿87,040.00
(R)-4-Isopropyl-2-(pyrimidin-2-yl)-4,5-dihydrooxazole
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Used in pharmaceutical synthesis as a chiral intermediate, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Its oxazoline core acts as a directing group in asymmetric catalysis, enabling selective carbon–carbon bond formation. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic peptide structures and enhance metabolic stability. Also utilized in agrochemicals for creating enantioselective herbi

Used in pharmaceutical synthesis as a chiral intermediate, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Its oxazoline core acts as a directing group in asymmetric catalysis, enabling selective carbon–carbon bond formation. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic peptide structures and enhance metabolic stability. Also utilized in agrochemicals for creating enantioselective herbicides and fungicides. Its pyrimidine moiety allows for hydrogen bonding interactions, improving target binding affinity in drug design.

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