2-Amino-1-Boc-imidazole
≥97%
- Product Code: 69168
CAS:
929568-19-4
Molecular Weight: | 183.21 g./mol | Molecular Formula: | C₈H₁₃N₃O₂ |
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EC Number: | MDL Number: | MFCD20702858 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
2-Amino-1-Boc-imidazole is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of drug candidates, where it serves as a key intermediate in the synthesis of imidazole-containing compounds. The Boc (tert-butoxycarbonyl) protecting group on the nitrogen atom allows for selective reactions to occur at other sites of the molecule, making it a versatile reagent in multi-step synthetic processes. Additionally, it finds application in the creation of biologically active molecules, such as kinase inhibitors and other therapeutic agents, due to the imidazole ring's ability to interact with biological targets. Its role in medicinal chemistry is significant, as it aids in the design and optimization of drugs with improved efficacy and selectivity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿5,700.00 |
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1.000 | 10-20 days | ฿15,200.00 |
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5.000 | 10-20 days | ฿50,000.00 |
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2-Amino-1-Boc-imidazole
2-Amino-1-Boc-imidazole is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of drug candidates, where it serves as a key intermediate in the synthesis of imidazole-containing compounds. The Boc (tert-butoxycarbonyl) protecting group on the nitrogen atom allows for selective reactions to occur at other sites of the molecule, making it a versatile reagent in multi-step synthetic processes. Additionally, it finds application in the creation of biologically active molecules, such as kinase inhibitors and other therapeutic agents, due to the imidazole ring's ability to interact with biological targets. Its role in medicinal chemistry is significant, as it aids in the design and optimization of drugs with improved efficacy and selectivity.
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