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

95%

Reagent Code: #231854
fingerprint
CAS Number 2757082-87-2

science Other reagents with same CAS 2757082-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.32 g/mol
Formula C₁₄H₂₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the development of agrochemicals and pharmaceuticals. Its structural features make it valuable in asymmetric synthesis, where the oxazole ring and chiral center contribute to stereoselective transformations. Commonly employed in the preparation of herbicides and plant growth regulators due to its stability and reactivity profile. Also utilized in research settings for designing novel catalysts and ligands in enantioselective reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,010.00
inventory 1g
10-20 days ฿46,030.00
$product.analytical_desc - NULL

Cart

No products

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

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the development of agrochemicals and pharmaceuticals. Its structural features make it valuable in asymmetric synthesis, where the oxazole ring and chiral center contribute to stereoselective transformations. Commonly employed in the preparation of herbicides and plant growth regulators due to its stability and reactivity profile. Also utilized in research settings for designing novel catalysts and ligands

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the development of agrochemicals and pharmaceuticals. Its structural features make it valuable in asymmetric synthesis, where the oxazole ring and chiral center contribute to stereoselective transformations. Commonly employed in the preparation of herbicides and plant growth regulators due to its stability and reactivity profile. Also utilized in research settings for designing novel catalysts and ligands in enantioselective reactions.

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...