2-Amino-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile

95%

Reagent Code: #42669
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CAS Number 23917-22-8

science Other reagents with same CAS 23917-22-8

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Weight 192.2807 g/mol
Formula C₁₀H₁₂N₂S
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MDL Number MFCD00121496
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a cyclohepta[b]thiophene core, makes it a valuable building block for developing compounds with potential therapeutic applications, particularly in the design of kinase inhibitors and other enzyme-targeting drugs. Researchers have explored its use in creating molecules that may exhibit anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its carbonitrile group provides a reactive site for further chemical modifications, enabling the development of diverse derivatives for drug discovery and optimization.

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inventory 250mg
10-20 days ฿1,683.00

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2-Amino-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a cyclohepta[b]thiophene core, makes it a valuable building block for developing compounds with potential therapeutic applications, particularly in the design of kinase inhibitors and other enzyme-targeting drugs. Researchers have explored its use in creating molecules that may exhibit anti-inflammatory, anticancer, or antimicrob

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a cyclohepta[b]thiophene core, makes it a valuable building block for developing compounds with potential therapeutic applications, particularly in the design of kinase inhibitors and other enzyme-targeting drugs. Researchers have explored its use in creating molecules that may exhibit anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its carbonitrile group provides a reactive site for further chemical modifications, enabling the development of diverse derivatives for drug discovery and optimization.

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