(R)-3-Amino-4-(tert-butoxy)butanoic acid
≥95%
- Product Code: 37621
CAS:
1956437-97-0
| Molecular Weight: | 175.23 g./mol | Molecular Formula: | C₈H₁₇NO₃ |
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| EC Number: | MDL Number: | MFCD30180243 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
(R)-3-Amino-4-(tert-butoxy)butanoic acid is primarily utilized in the field of organic synthesis as a chiral building block. Its structure, featuring both an amino group and a tert-butoxy group, makes it a valuable intermediate in the production of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, it is used in peptide synthesis and as a precursor for the preparation of complex molecules in medicinal chemistry. The tert-butoxy group provides steric protection, which can be advantageous in selective reactions, while the amino group allows for further functionalization, making it a versatile reagent in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,132.00 |
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| 0.250 | 10-20 days | ฿6,264.00 |
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(R)-3-Amino-4-(tert-butoxy)butanoic acid
(R)-3-Amino-4-(tert-butoxy)butanoic acid is primarily utilized in the field of organic synthesis as a chiral building block. Its structure, featuring both an amino group and a tert-butoxy group, makes it a valuable intermediate in the production of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, it is used in peptide synthesis and as a precursor for the preparation of complex molecules in medicinal chemistry. The tert-butoxy group provides steric protection, which can be advantageous in selective reactions, while the amino group allows for further functionalization, making it a versatile reagent in drug discovery and development processes.
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