N-(tert-Butyl)-2-((4,5-diphenyloxazol-2-yl)thio)propanamide

97%

Reagent Code: #54723
fingerprint
CAS Number 1385506-57-9

science Other reagents with same CAS 1385506-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 380.5032 g/mol
Formula C₂₂H₂₄N₂O₂S
badge Registry Numbers
MDL Number MFCD15659365
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting enzyme inhibition. Its structure, featuring an oxazole ring and thioether linkage, makes it valuable for designing compounds with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it is employed in the study of chemical reactions involving sulfur-containing compounds, aiding in the exploration of novel reaction pathways and mechanisms. Its stability and reactivity profile also make it suitable for use in material science, particularly in the synthesis of advanced polymers or coatings with specific functional properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,808.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(tert-Butyl)-2-((4,5-diphenyloxazol-2-yl)thio)propanamide
No image available

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting enzyme inhibition. Its structure, featuring an oxazole ring and thioether linkage, makes it valuable for designing compounds with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it is employed in the study of chemical reactions involving sulfur-con

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting enzyme inhibition. Its structure, featuring an oxazole ring and thioether linkage, makes it valuable for designing compounds with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it is employed in the study of chemical reactions involving sulfur-containing compounds, aiding in the exploration of novel reaction pathways and mechanisms. Its stability and reactivity profile also make it suitable for use in material science, particularly in the synthesis of advanced polymers or coatings with specific functional properties.

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...