3-(Boc-Amino)propylbromide
98%
- Product Code: 121403
CAS:
83948-53-2
Molecular Weight: | 238.12 g./mol | Molecular Formula: | C₈H₁₆BrNO₂ |
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EC Number: | MDL Number: | ||
Melting Point: | 37-39°C | Boiling Point: | |
Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a key reagent in organic synthesis, particularly in the preparation of complex molecules. It serves as a protected amine precursor, enabling the introduction of amine functionalities in multi-step reactions. The bromoalkyl group allows for alkylation reactions, making it useful for modifying nucleophiles such as amines, thiols, or alcohols. Commonly employed in peptide synthesis, where the Boc group provides temporary protection for amines during coupling reactions. Also utilized in the development of pharmaceutical compounds and bioconjugation strategies, where it acts as a linker or spacer to connect different molecular entities. Its versatility makes it valuable in creating intermediates for drug discovery and biochemical research.
Product Specification:
Test | Specification |
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Purity (%) | 98-100 |
Melting Point (Degree Celsius) | 37-39 |
Appearance | White Solid |
Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿300.00 |
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1.000 | 10-20 days | ฿360.00 |
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5.000 | 10-20 days | ฿560.00 |
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25.000 | 10-20 days | ฿1,650.00 |
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100.000 | 10-20 days | ฿6,400.00 |
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3-(Boc-Amino)propylbromide
Used as a key reagent in organic synthesis, particularly in the preparation of complex molecules. It serves as a protected amine precursor, enabling the introduction of amine functionalities in multi-step reactions. The bromoalkyl group allows for alkylation reactions, making it useful for modifying nucleophiles such as amines, thiols, or alcohols. Commonly employed in peptide synthesis, where the Boc group provides temporary protection for amines during coupling reactions. Also utilized in the development of pharmaceutical compounds and bioconjugation strategies, where it acts as a linker or spacer to connect different molecular entities. Its versatility makes it valuable in creating intermediates for drug discovery and biochemical research.
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