(3-Bromo-2-methyl-phenyl)-carbamic acid tert-butyl ester

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Reagent Code: #36682
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CAS Number 221538-03-0

science Other reagents with same CAS 221538-03-0

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Weight 286.1649 g/mol
Formula C₁₂H₁₆BrNO₂
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MDL Number MFCD11975627
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This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex chemical structures. It is often employed in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group serves as a protective group for the carbamic acid functionality. This protection allows for selective reactions to occur at other sites of the molecule without affecting the carbamic acid. Additionally, the bromine atom on the aromatic ring provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing diverse drug-like molecules. Its application is also seen in material science, where it can be used to modify polymers or create specialized coatings with specific properties.

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inventory 100mg
10-20 days ฿1,962.00

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(3-Bromo-2-methyl-phenyl)-carbamic acid tert-butyl ester
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This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex chemical structures. It is often employed in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group serves as a protective group for the carbamic acid functionality. This protection allows for selective reactions to occur at other sites of the molecule without affecting the carbamic acid. Additionally, the bromine atom

This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex chemical structures. It is often employed in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group serves as a protective group for the carbamic acid functionality. This protection allows for selective reactions to occur at other sites of the molecule without affecting the carbamic acid. Additionally, the bromine atom on the aromatic ring provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing diverse drug-like molecules. Its application is also seen in material science, where it can be used to modify polymers or create specialized coatings with specific properties.

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