1-(5-Bromo-4-chlorothiophen-2-yl)ethan-1-one

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Reagent Code: #39499
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CAS Number 123418-66-6

science Other reagents with same CAS 123418-66-6

blur_circular Chemical Specifications

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Weight 239.5174 g/mol
Formula C₆H₄BrClOS
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MDL Number MFCD11110669
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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 pharmaceutical industry, where it serves as a building block for the synthesis of potential drug candidates. Its structure, featuring both bromo and chloro substituents, allows for further functionalization through various chemical reactions, such as cross-coupling or nucleophilic substitution. Additionally, it is employed in agrochemical research for the creation of novel pesticides or herbicides, leveraging its heterocyclic thiophene core. Its versatility in chemical reactions makes it a useful component in material science for designing advanced organic materials with specific properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,212.00

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1-(5-Bromo-4-chlorothiophen-2-yl)ethan-1-one
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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 pharmaceutical industry, where it serves as a building block for the synthesis of potential drug candidates. Its structure, featuring both bromo and chloro substituents, allows for further functionalization through various chemical reactions, such as cross-coupling or nucleophilic substitution. Additionally, it is employed in agrochemic

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 pharmaceutical industry, where it serves as a building block for the synthesis of potential drug candidates. Its structure, featuring both bromo and chloro substituents, allows for further functionalization through various chemical reactions, such as cross-coupling or nucleophilic substitution. Additionally, it is employed in agrochemical research for the creation of novel pesticides or herbicides, leveraging its heterocyclic thiophene core. Its versatility in chemical reactions makes it a useful component in material science for designing advanced organic materials with specific properties.

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