Methyl 2-(chloromethyl)oxazole-4-carboxylate

≥95%

Reagent Code: #205538
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CAS Number 208465-72-9

science Other reagents with same CAS 208465-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.57 g/mol
Formula C₆H₆ClNO₃
badge Registry Numbers
MDL Number MFCD06660133
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating oxazole-based derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Commonly employed in research settings to build more complex molecules through nucleophilic substitution or coupling reactions. Also utilized in agrochemical research for designing novel pesticides or herbicides due to the oxazole ring’s metabolic stability and favorable electronic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,100.00
inventory 1g
10-20 days ฿2,530.00
inventory 5g
10-20 days ฿7,430.00
inventory 25g
10-20 days ฿21,820.00
Methyl 2-(chloromethyl)oxazole-4-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating oxazole-based derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Commonly employed in research settings to build more complex molecules through nucleophilic substitution or coupling reactions. Also utilized in agrochemical research for des

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating oxazole-based derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Commonly employed in research settings to build more complex molecules through nucleophilic substitution or coupling reactions. Also utilized in agrochemical research for designing novel pesticides or herbicides due to the oxazole ring’s metabolic stability and favorable electronic properties.

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