Methyl 2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)acetate

≥95%

  • Product Code: 41686
  CAS:    709665-73-6
Molecular Weight: 344.20 g./mol Molecular Formula: C₁₄H₁₈BrNO₄
EC Number: MDL Number: MFCD04115517
Melting Point: Boiling Point: 429.9°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This compound is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, where its bromophenyl and tert-butoxycarbonyl (Boc) protected amino groups make it valuable for constructing peptide-like structures. The Boc group provides temporary protection for the amine during synthesis, allowing selective reactions to occur at other sites. Additionally, the bromophenyl moiety can participate in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. This makes it a versatile building block for drug discovery and development, especially in the creation of bioactive compounds targeting specific biological pathways.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿2,853.00
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-
0.250 10-20 days ฿5,706.00
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-
Methyl 2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)acetate
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, where its bromophenyl and tert-butoxycarbonyl (Boc) protected amino groups make it valuable for constructing peptide-like structures. The Boc group provides temporary protection for the amine during synthesis, allowing selective reactions to occur at other sites. Additionally, the bromophenyl moiety can participate in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. This makes it a versatile building block for drug discovery and development, especially in the creation of bioactive compounds targeting specific biological pathways.
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