(S)-2-((tert-Butoxycarbonyl)amino)-2-(tetrahydro-2H-pyran-4-yl)acetic acid
95%
- Product Code: 38099
CAS:
711017-85-5
Molecular Weight: | 259.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₅ |
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EC Number: | MDL Number: | MFCD08272907 | |
Melting Point: | Boiling Point: | 423.5±20.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a building block in the preparation of complex molecules, particularly in the development of drugs targeting various diseases. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide chemistry, as the Boc group can be easily removed under mild acidic conditions without affecting other functional groups. Additionally, the tetrahydro-2H-pyran-4-yl moiety contributes to the molecule's stability and can influence the pharmacokinetic properties of the final drug product. It is commonly employed in medicinal chemistry research for designing and optimizing bioactive compounds.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,661.00 |
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0.250 | 10-20 days | ฿9,450.00 |
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1.000 | 10-20 days | ฿18,648.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-2-(tetrahydro-2H-pyran-4-yl)acetic acid
This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a building block in the preparation of complex molecules, particularly in the development of drugs targeting various diseases. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide chemistry, as the Boc group can be easily removed under mild acidic conditions without affecting other functional groups. Additionally, the tetrahydro-2H-pyran-4-yl moiety contributes to the molecule's stability and can influence the pharmacokinetic properties of the final drug product. It is commonly employed in medicinal chemistry research for designing and optimizing bioactive compounds.
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