CIS-3-BOC-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID
98%
- Product Code: 54817
CAS:
1006891-33-3
Molecular Weight: | 245.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₅ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 413.9±45.0℃(Predicted) | |
Density: | 1.19±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
CIS-3-BOC-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID is primarily used in organic synthesis as a key intermediate in the production of pharmaceuticals. Its structure makes it valuable in the development of drug candidates, particularly in the synthesis of compounds with therapeutic potential. The BOC (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions, enabling chemists to build complex molecules with precision. This chemical is often employed in the synthesis of peptides and peptidomimetics, which are crucial in drug discovery for targeting diseases such as cancer, infections, and neurological disorders. Additionally, its tetrahydropyran ring contributes to the stability and bioavailability of the resulting compounds, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $1,713.32 |
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CIS-3-BOC-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID
CIS-3-BOC-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID is primarily used in organic synthesis as a key intermediate in the production of pharmaceuticals. Its structure makes it valuable in the development of drug candidates, particularly in the synthesis of compounds with therapeutic potential. The BOC (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions, enabling chemists to build complex molecules with precision. This chemical is often employed in the synthesis of peptides and peptidomimetics, which are crucial in drug discovery for targeting diseases such as cancer, infections, and neurological disorders. Additionally, its tetrahydropyran ring contributes to the stability and bioavailability of the resulting compounds, making it a versatile building block in medicinal chemistry.
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