(R)-2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acid hydrate

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Reagent Code: #37453
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CAS Number 350230-37-4

science Other reagents with same CAS 350230-37-4

blur_circular Chemical Specifications

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Weight 223.22 g/mol
Formula C₈H₁₇NO₆
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a chiral building block in the production of enantiomerically pure drugs, particularly in the development of beta-amino acids and other bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is crucial in peptide chemistry, as it safeguards the amino group during synthesis and can be selectively removed under mild acidic conditions. The hydroxyl group allows for further functionalization, making it valuable in constructing complex molecular structures. Additionally, its chiral nature is exploited in asymmetric synthesis to achieve high stereochemical control in medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿333.00
inventory 25g
10-20 days ฿837.00
inventory 10g
10-20 days ฿396.00

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(R)-2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acid hydrate
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This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a chiral building block in the production of enantiomerically pure drugs, particularly in the development of beta-amino acids and other bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is crucial in peptide chemistry, as it safeguards the amino group during synthesis and can be selectively removed under mild acidic conditions. The hydroxyl group allows for further functionali

This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a chiral building block in the production of enantiomerically pure drugs, particularly in the development of beta-amino acids and other bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is crucial in peptide chemistry, as it safeguards the amino group during synthesis and can be selectively removed under mild acidic conditions. The hydroxyl group allows for further functionalization, making it valuable in constructing complex molecular structures. Additionally, its chiral nature is exploited in asymmetric synthesis to achieve high stereochemical control in medicinal chemistry applications.

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