2-Amino-4-ethyl-5-methylthiophene-3-carboxamide

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Reagent Code: #130787
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CAS Number 350996-89-3

science Other reagents with same CAS 350996-89-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.26 g/mol
Formula C₈H₁₂N₂OS
badge Registry Numbers
MDL Number MFCD01114969
thermostat Physical Properties
Boiling Point 270.8±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.236±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and anticancer agents. Its structure supports the formation of heterocyclic compounds with biological activity. Commonly employed in research settings for designing new drug candidates due to its ability to participate in cyclization and condensation reactions. Also utilized in agrochemicals for the development of novel pesticides with improved efficacy. Its amino and carboxamide groups allow for easy functionalization, making it valuable in combinatorial chemistry and high-throughput screening.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,770.00
inventory 1g
10-20 days ฿4,770.00
inventory 5g
10-20 days ฿16,720.00

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2-Amino-4-ethyl-5-methylthiophene-3-carboxamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and anticancer agents. Its structure supports the formation of heterocyclic compounds with biological activity. Commonly employed in research settings for designing new drug candidates due to its ability to participate in cyclization and condensation reactions. Also utilized in agrochemicals for the development of novel pesticides with improved efficacy. Its amino and carboxamide groups allow f

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and anticancer agents. Its structure supports the formation of heterocyclic compounds with biological activity. Commonly employed in research settings for designing new drug candidates due to its ability to participate in cyclization and condensation reactions. Also utilized in agrochemicals for the development of novel pesticides with improved efficacy. Its amino and carboxamide groups allow for easy functionalization, making it valuable in combinatorial chemistry and high-throughput screening.

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