tert-Butyl 6-(chloromethyl)-1H-indole-1-carboxylate

95%

Reagent Code: #49502
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CAS Number 1820685-06-0

science Other reagents with same CAS 1820685-06-0

blur_circular Chemical Specifications

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Weight 265.7300 g/mol
Formula C₁₄H₁₆NO₂Cl
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex indole derivatives. Its structure, featuring both a chloromethyl group and a tert-butyl carboxylate moiety, makes it particularly useful for further functionalization. It is often employed in the development of pharmaceutical compounds, where indole scaffolds are crucial due to their biological activity. Additionally, it serves as a key building block in the synthesis of agrochemicals and other fine chemicals. The chloromethyl group allows for easy modification through nucleophilic substitution reactions, enabling the attachment of various functional groups to the indole core.

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inventory 100mg
10-20 days ฿8,478.00

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tert-Butyl 6-(chloromethyl)-1H-indole-1-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex indole derivatives. Its structure, featuring both a chloromethyl group and a tert-butyl carboxylate moiety, makes it particularly useful for further functionalization. It is often employed in the development of pharmaceutical compounds, where indole scaffolds are crucial due to their biological activity. Additionally, it serves as a key building block in the synthesis of agrochemicals

This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex indole derivatives. Its structure, featuring both a chloromethyl group and a tert-butyl carboxylate moiety, makes it particularly useful for further functionalization. It is often employed in the development of pharmaceutical compounds, where indole scaffolds are crucial due to their biological activity. Additionally, it serves as a key building block in the synthesis of agrochemicals and other fine chemicals. The chloromethyl group allows for easy modification through nucleophilic substitution reactions, enabling the attachment of various functional groups to the indole core.

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