(S)-1-Benzyl 6-methyl 2-((tert-butoxycarbonyl)amino)-4-oxohexanedioate
97%
- Product Code: 57123
CAS:
630128-01-7
| Molecular Weight: | 379.40 g./mol | Molecular Formula: | C₁₉H₂₅NO₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30470618 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is commonly utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of peptide-based drugs, where its structure aids in the formation of specific amino acid sequences. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during synthesis, while the benzyl ester functionality allows for further modifications. Its application extends to the development of protease inhibitors and other bioactive compounds, making it valuable in medicinal chemistry research. Additionally, it is used in the preparation of chiral compounds, leveraging its stereochemistry to achieve high enantiomeric purity in final products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,880.00 |
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| 1.000 | 10-20 days | ฿7,200.00 |
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| 5.000 | 10-20 days | ฿25,344.00 |
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(S)-1-Benzyl 6-methyl 2-((tert-butoxycarbonyl)amino)-4-oxohexanedioate
This chemical is commonly utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of peptide-based drugs, where its structure aids in the formation of specific amino acid sequences. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during synthesis, while the benzyl ester functionality allows for further modifications. Its application extends to the development of protease inhibitors and other bioactive compounds, making it valuable in medicinal chemistry research. Additionally, it is used in the preparation of chiral compounds, leveraging its stereochemistry to achieve high enantiomeric purity in final products.
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