(S)-4-((Ethyl(phenyl)amino)methyl)-4,5-dihydrooxazol-2-amine

≥95%

Reagent Code: #237401
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CAS Number 1048346-74-2

science Other reagents with same CAS 1048346-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.28 g/mol
Formula C₁₂H₁₇N₃O
badge Registry Numbers
MDL Number MFCD22493512
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and asymmetric synthesis. Its amine and oxazoline functionalities make it valuable for catalyzing enantioselective reactions, especially in the preparation of nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and ability to form stable complexes with metal catalysts.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,520.00
inventory 10mg
10-20 days ฿17,080.00
inventory 25mg
10-20 days ฿38,080.00
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(S)-4-((Ethyl(phenyl)amino)methyl)-4,5-dihydrooxazol-2-amine
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and asymmetric synthesis. Its amine and oxazoline functionalities make it valuable for catalyzing enantioselective reactions, especially in the preparation of nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and ability to form stable complexes with metal catalysts.

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and asymmetric synthesis. Its amine and oxazoline functionalities make it valuable for catalyzing enantioselective reactions, especially in the preparation of nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and ability to form stable complexes with metal catalysts.

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