Methyl 4-bromo-5-methoxythiophene-2-carboxylate

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Reagent Code: #47498
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CAS Number 1047630-22-7

science Other reagents with same CAS 1047630-22-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.0977 g/mol
Formula C₇H₇BrO₃S
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MDL Number MFCD30736615
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Methyl 4-bromo-5-methoxythiophene-2-carboxylate is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a methyl carboxylate ester along with bromo and methoxy groups on a thiophene ring, makes it valuable in the construction of heterocyclic compounds, particularly in pharmaceutical and agrochemical research. It serves as an intermediate in the synthesis of potential drug candidates, especially those targeting neurological and inflammatory diseases. Additionally, its multiple reactive functional groups allow for further selective functionalization, enabling the creation of diverse chemical libraries for screening and discovery purposes. In material science, it can be employed in the design of organic semiconductors or conductive polymers due to the thiophene backbone, which is known for its electronic properties.

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inventory 100mg
10-20 days ฿5,445.00

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Methyl 4-bromo-5-methoxythiophene-2-carboxylate
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Methyl 4-bromo-5-methoxythiophene-2-carboxylate is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a methyl carboxylate ester along with bromo and methoxy groups on a thiophene ring, makes it valuable in the construction of heterocyclic compounds, particularly in pharmaceutical and agrochemical research. It serves as an intermediate in the synthesis of potential drug candidates, especially those targeting neurol

Methyl 4-bromo-5-methoxythiophene-2-carboxylate is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a methyl carboxylate ester along with bromo and methoxy groups on a thiophene ring, makes it valuable in the construction of heterocyclic compounds, particularly in pharmaceutical and agrochemical research. It serves as an intermediate in the synthesis of potential drug candidates, especially those targeting neurological and inflammatory diseases. Additionally, its multiple reactive functional groups allow for further selective functionalization, enabling the creation of diverse chemical libraries for screening and discovery purposes. In material science, it can be employed in the design of organic semiconductors or conductive polymers due to the thiophene backbone, which is known for its electronic properties.

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