trans-4-(tert-Butoxycarbonylamino)cyclohexanol
98%
- Product Code: 58614
CAS:
111300-06-2
| Molecular Weight: | 215.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03844613 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of drugs, particularly in the synthesis of active pharmaceutical ingredients (APIs). The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Additionally, it finds application in the production of peptides and peptidomimetics, where the Boc group can be easily removed under mild acidic conditions without disrupting other sensitive functional groups. Its cyclohexanol moiety also contributes to its use in the design of compounds with specific stereochemical and conformational properties, which are essential in drug discovery and development.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5-100 |
| Appearance | White to Light Yellow Crystals Powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿420.00 |
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| 5.000 | 10-20 days | ฿1,030.00 |
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| 25.000 | 10-20 days | ฿2,790.00 |
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trans-4-(tert-Butoxycarbonylamino)cyclohexanol
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of drugs, particularly in the synthesis of active pharmaceutical ingredients (APIs). The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Additionally, it finds application in the production of peptides and peptidomimetics, where the Boc group can be easily removed under mild acidic conditions without disrupting other sensitive functional groups. Its cyclohexanol moiety also contributes to its use in the design of compounds with specific stereochemical and conformational properties, which are essential in drug discovery and development.
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