(2R,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride
95%
- Product Code: 70846
CAS:
1161931-71-0
Molecular Weight: | 252.74 g./mol | Molecular Formula: | C₁₀H₂₁ClN₂O₃ |
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EC Number: | MDL Number: | MFCD11101163 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is widely used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring both a Boc-protected amine and a hydroxymethyl group, makes it a valuable building block for creating complex molecules with specific stereochemistry. It is often employed in the production of antiviral and anticancer agents, where precise stereochemical control is critical for efficacy. Additionally, it serves as a key intermediate in the synthesis of peptidomimetics and other biologically active compounds, aiding in the exploration of new therapeutic targets. Its hydrochloride form enhances stability and solubility, facilitating its use in various chemical reactions and drug development processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,211.00 |
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0.250 | 10-20 days | ฿8,307.00 |
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1.000 | 10-20 days | ฿20,889.00 |
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(2R,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride
This compound is widely used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring both a Boc-protected amine and a hydroxymethyl group, makes it a valuable building block for creating complex molecules with specific stereochemistry. It is often employed in the production of antiviral and anticancer agents, where precise stereochemical control is critical for efficacy. Additionally, it serves as a key intermediate in the synthesis of peptidomimetics and other biologically active compounds, aiding in the exploration of new therapeutic targets. Its hydrochloride form enhances stability and solubility, facilitating its use in various chemical reactions and drug development processes.
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