Methyl 5-(3,3-dimethyl-1-butyn-1-yl)-3-iodo-2-thiophenecarboxylate

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Reagent Code: #50405
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CAS Number 1263098-97-0

science Other reagents with same CAS 1263098-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.2 g/mol
Formula C₁₂H₁₃IO₂S
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of complex molecules. It is particularly valuable in the construction of thiophene-based structures, which are prevalent in pharmaceuticals and agrochemicals. The presence of the iodine atom allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its alkyne group enables click chemistry applications, facilitating the creation of targeted drug delivery systems or bioactive compounds. Its role in material science is also notable, contributing to the synthesis of organic semiconductors and conductive polymers.

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inventory 1g
10-20 days ฿31,500.00

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Methyl 5-(3,3-dimethyl-1-butyn-1-yl)-3-iodo-2-thiophenecarboxylate
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Used primarily in organic synthesis, this compound serves as a key intermediate in the development of complex molecules. It is particularly valuable in the construction of thiophene-based structures, which are prevalent in pharmaceuticals and agrochemicals. The presence of the iodine atom allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its alkyne group enables click chemistry applications, facilitating the c

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of complex molecules. It is particularly valuable in the construction of thiophene-based structures, which are prevalent in pharmaceuticals and agrochemicals. The presence of the iodine atom allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its alkyne group enables click chemistry applications, facilitating the creation of targeted drug delivery systems or bioactive compounds. Its role in material science is also notable, contributing to the synthesis of organic semiconductors and conductive polymers.

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