Methyl 4-iodo-1,2-thiazole-3-carboxylate

95%

Reagent Code: #130890
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CAS Number 397329-61-2

science Other reagents with same CAS 397329-61-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.06 g/mol
Formula C₅H₄INO₂S
badge Registry Numbers
MDL Number MFCD29060514
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antimicrobial and anti-inflammatory properties. Its structure allows for further functionalization in heterocyclic chemistry, making it valuable in medicinal chemistry research. Commonly employed in cross-coupling reactions to introduce the thiazole moiety into target molecules, aiding in the creation of novel drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactive iodine group and stable heterocyclic core.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,460.00
inventory 1g
10-20 days ฿28,220.00
inventory 100mg
10-20 days ฿6,160.00
Methyl 4-iodo-1,2-thiazole-3-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antimicrobial and anti-inflammatory properties. Its structure allows for further functionalization in heterocyclic chemistry, making it valuable in medicinal chemistry research. Commonly employed in cross-coupling reactions to introduce the thiazole moiety into target molecules, aiding in the creation of novel drug candidates. Also utilized in agrochemical research f

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antimicrobial and anti-inflammatory properties. Its structure allows for further functionalization in heterocyclic chemistry, making it valuable in medicinal chemistry research. Commonly employed in cross-coupling reactions to introduce the thiazole moiety into target molecules, aiding in the creation of novel drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactive iodine group and stable heterocyclic core.

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