1-(Boc-amino)-3-(isopropylamino)propane
≥97%
- Product Code: 69164
CAS:
1229627-05-7
Molecular Weight: | 216.32 g./mol | Molecular Formula: | C₁₁H₂₄N₂O₂ |
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EC Number: | MDL Number: | MFCD12828784 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the synthesis of compounds that target specific biological pathways, such as enzyme inhibitors or receptor modulators. The Boc (tert-butyloxycarbonyl) group provides protection for the amine functionality during multi-step reactions, allowing selective deprotection at a later stage. The isopropylamino moiety can impart specific steric and electronic properties to the final molecule, influencing its binding affinity and selectivity. It is often employed in the development of drugs for neurological disorders, cancer, and cardiovascular diseases due to its ability to modulate key biological targets. Additionally, it finds use in peptide chemistry for the controlled assembly of peptide chains.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $202.06 |
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1.000 | 10-20 days | $504.92 |
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1-(Boc-amino)-3-(isopropylamino)propane
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the synthesis of compounds that target specific biological pathways, such as enzyme inhibitors or receptor modulators. The Boc (tert-butyloxycarbonyl) group provides protection for the amine functionality during multi-step reactions, allowing selective deprotection at a later stage. The isopropylamino moiety can impart specific steric and electronic properties to the final molecule, influencing its binding affinity and selectivity. It is often employed in the development of drugs for neurological disorders, cancer, and cardiovascular diseases due to its ability to modulate key biological targets. Additionally, it finds use in peptide chemistry for the controlled assembly of peptide chains.
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