Ethyl 2-bromo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

95%

Reagent Code: #43206
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CAS Number 150108-66-0

science Other reagents with same CAS 150108-66-0

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Weight 289.1887 g/mol
Formula C₁₁H₁₃BrO₂S
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MDL Number MFCD19441937
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This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for creating potential drug candidates. Its structure, featuring a bromine atom and an ester group, allows for versatile reactivity, enabling modifications through various chemical reactions such as nucleophilic substitution and cross-coupling reactions. Researchers often employ it in the construction of thiophene-based molecules, which are known for their applications in pharmaceuticals, agrochemicals, and materials science. Additionally, it can serve as a precursor for the synthesis of biologically active molecules, including those with potential anti-inflammatory, antimicrobial, or anticancer properties.

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inventory 100mg
10-20 days ฿6,255.00

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Ethyl 2-bromo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
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This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for creating potential drug candidates. Its structure, featuring a bromine atom and an ester group, allows for versatile reactivity, enabling modifications through various chemical reactions such as nucleophilic substitution and cross-coupling reactions. Res

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical structures. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for creating potential drug candidates. Its structure, featuring a bromine atom and an ester group, allows for versatile reactivity, enabling modifications through various chemical reactions such as nucleophilic substitution and cross-coupling reactions. Researchers often employ it in the construction of thiophene-based molecules, which are known for their applications in pharmaceuticals, agrochemicals, and materials science. Additionally, it can serve as a precursor for the synthesis of biologically active molecules, including those with potential anti-inflammatory, antimicrobial, or anticancer properties.

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