(S)-2-(2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinolin-3-yl)acetic acid
95%
- Product Code: 86910
CAS:
270062-98-1
| Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861031 | |
| Melting Point: | Boiling Point: | 454.5±38.0 °C(Predicted) | |
| Density: | 1.180 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those targeting neurological and cardiovascular diseases. Its structure is often employed in the preparation of tetrahydroisoquinoline derivatives, which are known for their biological activity. Additionally, it is used in peptide chemistry for the introduction of specific functional groups, aiding in the creation of peptide-based drugs. Its tert-butoxycarbonyl (Boc) protecting group makes it valuable in multi-step synthetic processes, ensuring selective reactivity and stability during reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,528.00 |
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| 0.250 | 10-20 days | ฿5,247.00 |
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| 1.000 | 10-20 days | ฿13,050.00 |
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(S)-2-(2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinolin-3-yl)acetic acid
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those targeting neurological and cardiovascular diseases. Its structure is often employed in the preparation of tetrahydroisoquinoline derivatives, which are known for their biological activity. Additionally, it is used in peptide chemistry for the introduction of specific functional groups, aiding in the creation of peptide-based drugs. Its tert-butoxycarbonyl (Boc) protecting group makes it valuable in multi-step synthetic processes, ensuring selective reactivity and stability during reactions.
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