1-(Boc-amino)-3-(methylamino)propane Hydrochloride
≥95%
- Product Code: 69156
CAS:
1188264-02-9
| Molecular Weight: | 224.73 g./mol | Molecular Formula: | C₉H₂₁ClN₂O₂ |
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| EC Number: | MDL Number: | MFCD11101326 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
1-(Boc-amino)-3-(methylamino)propane Hydrochloride is primarily used in organic synthesis as a key intermediate in the preparation of more complex molecules. It is particularly valuable in peptide chemistry, where the Boc (tert-butoxycarbonyl) group serves as a protective group for amines during the synthesis process. This compound is often employed in the development of pharmaceuticals, enabling the controlled assembly of amino acids and other building blocks to create biologically active compounds. Its role in protecting amines ensures selective reactions, which is crucial for the precise construction of target molecules in drug discovery and development. Additionally, it finds application in the synthesis of small molecule inhibitors and other bioactive agents, contributing to advancements in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,744.00 |
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| 5.000 | 10-20 days | ฿12,438.00 |
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1-(Boc-amino)-3-(methylamino)propane Hydrochloride
1-(Boc-amino)-3-(methylamino)propane Hydrochloride is primarily used in organic synthesis as a key intermediate in the preparation of more complex molecules. It is particularly valuable in peptide chemistry, where the Boc (tert-butoxycarbonyl) group serves as a protective group for amines during the synthesis process. This compound is often employed in the development of pharmaceuticals, enabling the controlled assembly of amino acids and other building blocks to create biologically active compounds. Its role in protecting amines ensures selective reactions, which is crucial for the precise construction of target molecules in drug discovery and development. Additionally, it finds application in the synthesis of small molecule inhibitors and other bioactive agents, contributing to advancements in medicinal chemistry.
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