Ethyl 2-amino-4-(trifluoromethyl)oxazole-5-carboxylate

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Reagent Code: #183998
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CAS Number 135026-17-4

science Other reagents with same CAS 135026-17-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.14 g/mol
Formula C₇H₇F₃N₂O₃
badge Registry Numbers
MDL Number MFCD09909738
inventory_2 Storage & Handling
Storage Keep away from light, dry, 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the construction of heterocyclic compounds with potential antimicrobial, antifungal, and insecticidal properties. Commonly employed in medicinal chemistry for scaffold modification due to the presence of reactive amino and ester groups, enabling further functionalization. Also utilized in the preparation of fluorinated analogs to enhance metabolic stability and lipophilicity in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,690.00
inventory 1g
10-20 days ฿9,870.00
inventory 5g
10-20 days ฿29,760.00
inventory 250mg
10-20 days ฿5,270.00
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Ethyl 2-amino-4-(trifluoromethyl)oxazole-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the construction of heterocyclic compounds with potential antimicrobial, antifungal, and insecticidal properties. Commonly employed in medicinal chemistry for scaffold modification due to the presence of reactive amino and ester groups, enabling further functionalization. Also utilized in the preparation of fluorinated analogs to enhance metaboli

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the construction of heterocyclic compounds with potential antimicrobial, antifungal, and insecticidal properties. Commonly employed in medicinal chemistry for scaffold modification due to the presence of reactive amino and ester groups, enabling further functionalization. Also utilized in the preparation of fluorinated analogs to enhance metabolic stability and lipophilicity in drug candidates.

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