Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylate

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Reagent Code: #203451
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CAS Number 349662-62-0

science Other reagents with same CAS 349662-62-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.22 g/mol
Formula C₇H₉NO₃S
badge Registry Numbers
MDL Number MFCD20696628
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in the preparation of kinase inhibitors and other biologically active molecules. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactive functional groups. Serves as a building block in combinatorial chemistry for high-throughput screening libraries.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,330.00
inventory 1g
10-20 days ฿19,530.00
inventory 5g
10-20 days ฿65,100.00
Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in the preparation of kinase inhibitors and other biologically active molecules. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactive functional groups. Serves as a building b

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in the preparation of kinase inhibitors and other biologically active molecules. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactive functional groups. Serves as a building block in combinatorial chemistry for high-throughput screening libraries.

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