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 |
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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 |
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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 |
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1.000 | 10-20 days | ฿290.00 |
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5.000 | 10-20 days | ฿760.00 |
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25.000 | 10-20 days | ฿2,280.00 |
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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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