1-(5-(3-azidoazetidine-1-carbonyl)thiophen-2-yl)ethan-1-one

95%

Reagent Code: #123838
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CAS Number 2098066-31-8

science Other reagents with same CAS 2098066-31-8

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Weight 250.28 g/mol
Formula C₁₀H₁₀N₄O₂S
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description Product Description

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of novel pharmaceuticals, particularly in the design of molecules with potential therapeutic properties. The presence of the azido group makes it valuable for click chemistry applications, enabling efficient and selective reactions with alkynes to form triazole derivatives. These derivatives are often explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory effects. Additionally, its thiophene moiety contributes to its use in the synthesis of organic electronic materials, where it can enhance conductivity and stability in devices such as organic field-effect transistors (OFETs) and solar cells.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,074.00
inventory 250mg
10-20 days ฿47,430.00

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1-(5-(3-azidoazetidine-1-carbonyl)thiophen-2-yl)ethan-1-one
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This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of novel pharmaceuticals, particularly in the design of molecules with potential therapeutic properties. The presence of the azido group makes it valuable for click chemistry applications, enabling efficient and selective reactions with alkynes to form triazole derivatives. These derivatives are often explored for their biological activities, including antimicr

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of novel pharmaceuticals, particularly in the design of molecules with potential therapeutic properties. The presence of the azido group makes it valuable for click chemistry applications, enabling efficient and selective reactions with alkynes to form triazole derivatives. These derivatives are often explored for their biological activities, including antimicrobial, anticancer, and anti-inflammatory effects. Additionally, its thiophene moiety contributes to its use in the synthesis of organic electronic materials, where it can enhance conductivity and stability in devices such as organic field-effect transistors (OFETs) and solar cells.

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