(2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride

95%

Reagent Code: #36552
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CAS Number 1279038-32-2

science Other reagents with same CAS 1279038-32-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.74 g/mol
Formula C₁₀H₂₁ClN₂O₃
badge Registry Numbers
MDL Number MFCD11101172
inventory_2 Storage & Handling
Storage 2-8℃, dry, airtight

description Product Description

This compound is primarily used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex molecules. Its structure, featuring a hydroxymethyl group, a free amino group at the 4-position, and a Boc-protected pyrrolidine nitrogen with (2S,4R) stereochemistry, makes it valuable for constructing chiral centers in drug development. It is often employed in the creation of antiviral and anticancer agents, where precise stereochemistry is crucial for biological activity. Additionally, it serves as a building block in peptide chemistry, enabling the formation of specific peptide bonds. Its Boc-protected amine group allows for selective deprotection, facilitating controlled reactions in multi-step synthetic processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿40,000.00
inventory 250mg
10-20 days ฿64,000.00
inventory 1g
10-20 days ฿31,374.00
inventory 500mg
10-20 days ฿104,000.00

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(2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride
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This compound is primarily used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex molecules. Its structure, featuring a hydroxymethyl group, a free amino group at the 4-position, and a Boc-protected pyrrolidine nitrogen with (2S,4R) stereochemistry, makes it valuable for constructing chiral centers in drug development. It is often employed in the creation of antiviral and anticancer agents, where precise stereochemistry is crucial for biological activity. A

This compound is primarily used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex molecules. Its structure, featuring a hydroxymethyl group, a free amino group at the 4-position, and a Boc-protected pyrrolidine nitrogen with (2S,4R) stereochemistry, makes it valuable for constructing chiral centers in drug development. It is often employed in the creation of antiviral and anticancer agents, where precise stereochemistry is crucial for biological activity. Additionally, it serves as a building block in peptide chemistry, enabling the formation of specific peptide bonds. Its Boc-protected amine group allows for selective deprotection, facilitating controlled reactions in multi-step synthetic processes.

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