(S)-1-tert-Butyl 4-methyl 2-aminosuccinate hydrochloride
97%
- Product Code: 37975
CAS:
34582-30-4
| Molecular Weight: | 239.70 g./mol | Molecular Formula: | C₉H₁₈ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05662354 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring both tert-butyl and methyl ester groups, makes it a valuable building block for creating enantiomerically pure compounds. It is often employed in asymmetric synthesis to produce amino acid derivatives, which are crucial in the design of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its hydrochloride form enhances solubility, facilitating its use in various organic reactions and purification processes. The compound’s stability and reactivity also make it suitable for research in peptide chemistry and medicinal chemistry, where precise stereochemical control is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿360.00 |
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| 1.000 | 10-20 days | ฿396.00 |
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| 5.000 | 10-20 days | ฿1,629.00 |
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| 10.000 | 10-20 days | ฿2,835.00 |
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(S)-1-tert-Butyl 4-methyl 2-aminosuccinate hydrochloride
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring both tert-butyl and methyl ester groups, makes it a valuable building block for creating enantiomerically pure compounds. It is often employed in asymmetric synthesis to produce amino acid derivatives, which are crucial in the design of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its hydrochloride form enhances solubility, facilitating its use in various organic reactions and purification processes. The compound’s stability and reactivity also make it suitable for research in peptide chemistry and medicinal chemistry, where precise stereochemical control is essential.
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