(R)-2-((tert-Butoxycarbonyl)amino)-2-phenylethyl methanesulfonate
98%
- Product Code: 113474
CAS:
102089-75-8
Molecular Weight: | 315.39 g./mol | Molecular Formula: | C₁₄H₂₁NO₅S |
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EC Number: | MDL Number: | MFCD22571103 | |
Melting Point: | 112-114 °C | Boiling Point: | 497.2±45.0 °C(Predicted) |
Density: | 1.204±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily used in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, where the (R)-configuration is essential for biological activity. Its methanesulfonate group makes it a suitable substrate for nucleophilic substitution reactions, enabling the introduction of various functional groups. Additionally, it is utilized in peptide coupling reactions, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, ensuring selective reactions in complex molecular constructions. Its application is critical in the development of targeted therapies and bioactive molecules.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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100.000 | 10-20 days | ฿3,861.00 |
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5.000 | 10-20 days | ฿342.00 |
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25.000 | 10-20 days | ฿1,170.00 |
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(R)-2-((tert-Butoxycarbonyl)amino)-2-phenylethyl methanesulfonate
This chemical is primarily used in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, where the (R)-configuration is essential for biological activity. Its methanesulfonate group makes it a suitable substrate for nucleophilic substitution reactions, enabling the introduction of various functional groups. Additionally, it is utilized in peptide coupling reactions, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, ensuring selective reactions in complex molecular constructions. Its application is critical in the development of targeted therapies and bioactive molecules.
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