(R)-2-((tert-Butoxycarbonyl)amino)-2-phenylethyl methanesulfonate
98%
Reagent
Code: #113474
CAS Number
102089-75-8
science Other reagents with same CAS 102089-75-8
blur_circular Chemical Specifications
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Molecular Information
Weight
315.39 g/mol
Formula
C₁₄H₂₁NO₅S
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Registry Numbers
MDL Number
MFCD22571103
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Physical Properties
Melting Point
112-114 °C
Boiling Point
497.2±45.0 °C(Predicted)
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Storage & Handling
Density
1.204±0.06 g/cm3(Predicted)
Storage
2-8°C, sealed, dry
description 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.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| APPEARANCE | White to off-white solid |
| Purity (%) | 97.5-100 |
| OR(C=1.00g/100ml CHCL3) | -24.5--20.5 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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