tert-butyl 2-oxoazepane-1-carboxylate

95%

  • Product Code: 84428
  CAS:    106412-36-6
Molecular Weight: 213.27 g./mol Molecular Formula: C₁₁H₁₉NO₃
EC Number: MDL Number: MFCD03265235
Melting Point: 35-37 °C Boiling Point:
Density: 1.038 g/cm3(Predicted) Storage Condition: room temperature
Product Description: This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butyl ester and an azepane ring, makes it a useful building block for constructing nitrogen-containing heterocycles, which are common in drug molecules. Additionally, it is employed in the synthesis of peptidomimetics and other bioactive compounds, where the azepane ring can mimic peptide structures or serve as a scaffold for drug design. Its stability and reactivity under various conditions allow for its use in multi-step synthetic routes, making it a key component in the production of therapeutic agents targeting neurological disorders, cardiovascular diseases, and other medical conditions.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿2,700.00
+
-
0.250 10-20 days ฿5,283.00
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-
1.000 10-20 days ฿10,638.00
+
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tert-butyl 2-oxoazepane-1-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). Its structure, featuring both a tert-butyl ester and an azepane ring, makes it a useful building block for constructing nitrogen-containing heterocycles, which are common in drug molecules. Additionally, it is employed in the synthesis of peptidomimetics and other bioactive compounds, where the azepane ring can mimic peptide structures or serve as a scaffold for drug design. Its stability and reactivity under various conditions allow for its use in multi-step synthetic routes, making it a key component in the production of therapeutic agents targeting neurological disorders, cardiovascular diseases, and other medical conditions.
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