1-Boc-3-azetidinone

97%

  • Product Code: 114541
  Alias:    tert-butyl 3-oxoazetidine-1-carboxylate
  CAS:    398489-26-4
Molecular Weight: 171.19 g./mol Molecular Formula: C₈H₁₃NO₃
EC Number: MDL Number: MFCD01861741
Melting Point: 49-52°C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: 1-Boc-3-azetidinone is widely used in organic synthesis as a key intermediate for the preparation of various pharmaceutical compounds. It is particularly valuable in the development of β-lactam antibiotics, where it serves as a building block for constructing the azetidinone ring, a core structure in many antibiotics. Additionally, it is employed in the synthesis of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. The Boc (tert-butoxycarbonyl) protecting group in this compound allows for selective reactions, making it a versatile tool in multi-step synthetic processes. Its application extends to the production of other nitrogen-containing heterocycles, which are important in medicinal chemistry for designing drugs with enhanced efficacy and specificity.
Product Specification:
Test Specification
Melting Point 50-54
Purity (GC) 97-100
Appearance White To Tan Solid
Infrared Spectrum Conforms To Structure
Note This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid)
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $14.57
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5.000 10-20 days $38.17
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25.000 10-20 days $114.52
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1-Boc-3-azetidinone
1-Boc-3-azetidinone is widely used in organic synthesis as a key intermediate for the preparation of various pharmaceutical compounds. It is particularly valuable in the development of β-lactam antibiotics, where it serves as a building block for constructing the azetidinone ring, a core structure in many antibiotics. Additionally, it is employed in the synthesis of protease inhibitors, which are crucial in treating diseases such as HIV and hepatitis C. The Boc (tert-butoxycarbonyl) protecting group in this compound allows for selective reactions, making it a versatile tool in multi-step synthetic processes. Its application extends to the production of other nitrogen-containing heterocycles, which are important in medicinal chemistry for designing drugs with enhanced efficacy and specificity.
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