Methyl 5-bromo-2-(dibromomethyl)benzoate

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Reagent Code: #48888
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CAS Number 1265286-99-4

science Other reagents with same CAS 1265286-99-4

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Weight 386.8627 g/mol
Formula C₉H₇Br₃O₂
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MDL Number MFCD25121753
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This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure features an aryl bromide at the 5-position, a dibromomethyl group at the 2-position, and a methyl benzoate ester, making it particularly useful in the development of pharmaceutical intermediates. The aryl bromine enables further functionalization through various coupling reactions, such as Suzuki or Heck reactions, for creating diverse aromatic compounds. The dibromomethyl group (-CHBr2) can be readily converted to an aldehyde via hydrolysis, providing access to additional synthetic pathways. Additionally, it can be employed in the synthesis of agrochemicals, where its reactive sites facilitate incorporation into larger, biologically active structures. The ester group offers opportunities for hydrolysis or transesterification, expanding its utility in fine chemical manufacturing.

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inventory 250mg
10-20 days ฿3,078.00

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Methyl 5-bromo-2-(dibromomethyl)benzoate
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This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure features an aryl bromide at the 5-position, a dibromomethyl group at the 2-position, and a methyl benzoate ester, making it particularly useful in the development of pharmaceutical intermediates. The aryl bromine enables further functionalization through various coupling reactions, such as Suzuki or Heck reactions, for creating diverse aromatic compounds. The

This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure features an aryl bromide at the 5-position, a dibromomethyl group at the 2-position, and a methyl benzoate ester, making it particularly useful in the development of pharmaceutical intermediates. The aryl bromine enables further functionalization through various coupling reactions, such as Suzuki or Heck reactions, for creating diverse aromatic compounds. The dibromomethyl group (-CHBr2) can be readily converted to an aldehyde via hydrolysis, providing access to additional synthetic pathways. Additionally, it can be employed in the synthesis of agrochemicals, where its reactive sites facilitate incorporation into larger, biologically active structures. The ester group offers opportunities for hydrolysis or transesterification, expanding its utility in fine chemical manufacturing.

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