3-hydrazinyl-2-methyl-7,8-dihydro-6H-cyclopenta[2,3]thieno[2,4-b]pyrimidin-1-one

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Reagent Code: #245606
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CAS Number 351342-00-2

science Other reagents with same CAS 351342-00-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.29 g/mol
Formula C₁₀H₁₂N₄OS
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical research as a key intermediate for synthesizing bioactive molecules, particularly in the development of kinase inhibitors and antitumor agents. Its hydrazine functionality allows for easy derivatization, enabling the formation of hydrazone or azole structures that enhance binding to biological targets. Also explored in medicinal chemistry for designing compounds with anti-inflammatory and antimicrobial properties. Additionally, serves as a building block in heterocyclic synthesis due to its fused ring system and reactive side chain.

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inventory 5mg
10-20 days ฿29,690.00

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3-hydrazinyl-2-methyl-7,8-dihydro-6H-cyclopenta[2,3]thieno[2,4-b]pyrimidin-1-one
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Used in pharmaceutical research as a key intermediate for synthesizing bioactive molecules, particularly in the development of kinase inhibitors and antitumor agents. Its hydrazine functionality allows for easy derivatization, enabling the formation of hydrazone or azole structures that enhance binding to biological targets. Also explored in medicinal chemistry for designing compounds with anti-inflammatory and antimicrobial properties. Additionally, serves as a building block in heterocyclic synthesis d

Used in pharmaceutical research as a key intermediate for synthesizing bioactive molecules, particularly in the development of kinase inhibitors and antitumor agents. Its hydrazine functionality allows for easy derivatization, enabling the formation of hydrazone or azole structures that enhance binding to biological targets. Also explored in medicinal chemistry for designing compounds with anti-inflammatory and antimicrobial properties. Additionally, serves as a building block in heterocyclic synthesis due to its fused ring system and reactive side chain.

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