Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid
99%
- Product Code: 36218
CAS:
1353893-22-7
| Molecular Weight: | 393.43 g./mol | Molecular Formula: | C₁₆H₃₁N₃O₈ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid is primarily utilized in the field of organic synthesis and medicinal chemistry. Its unique structure, featuring an azido group and a dimethylamino carbonyl moiety, makes it a valuable intermediate in the development of complex molecules, particularly in the synthesis of pharmaceuticals. The azido group is often employed in click chemistry reactions, enabling the formation of triazole linkages, which are crucial in drug discovery and bioconjugation processes. Additionally, the dimethylamino carbonyl group can serve as a precursor for further functionalization, aiding in the creation of bioactive compounds. This chemical is also explored in the design of enzyme inhibitors and receptor ligands, where its stereochemistry and functional groups play a critical role in binding interactions. Its oxalic acid component further enhances its utility in crystallization and purification processes, making it a versatile tool in chemical research and development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White powder |
| PURITY | 99-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,360.00 |
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| 5.000 | 10-20 days | ฿4,320.00 |
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| 25.000 | 10-20 days | ฿13,680.00 |
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Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid is primarily utilized in the field of organic synthesis and medicinal chemistry. Its unique structure, featuring an azido group and a dimethylamino carbonyl moiety, makes it a valuable intermediate in the development of complex molecules, particularly in the synthesis of pharmaceuticals. The azido group is often employed in click chemistry reactions, enabling the formation of triazole linkages, which are crucial in drug discovery and bioconjugation processes. Additionally, the dimethylamino carbonyl group can serve as a precursor for further functionalization, aiding in the creation of bioactive compounds. This chemical is also explored in the design of enzyme inhibitors and receptor ligands, where its stereochemistry and functional groups play a critical role in binding interactions. Its oxalic acid component further enhances its utility in crystallization and purification processes, making it a versatile tool in chemical research and development.
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