(R)-2-((tert-Butoxycarbonyl)amino)propanoic acid hydrate

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Reagent Code: #37465
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CAS Number 75638-15-2

science Other reagents with same CAS 75638-15-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.22 g/mol
Formula C₈H₁₇NO₅
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MDL Number MFCD26383924
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. Its tert-butoxycarbonyl (Boc) group protects the amino functionality during chemical reactions, allowing selective modification of other parts of the molecule. It is particularly valuable in solid-phase peptide synthesis (SPPS), a method widely employed to produce peptides with high purity and specificity. Additionally, it finds application in the development of chiral compounds and bioactive molecules, where its stereochemistry plays a crucial role in ensuring the desired biological activity. The hydrate form ensures stability and ease of handling during storage and use in laboratory settings.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿720.00
inventory 1g
10-20 days ฿360.00

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(R)-2-((tert-Butoxycarbonyl)amino)propanoic acid hydrate
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This compound is primarily used in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. Its tert-butoxycarbonyl (Boc) group protects the amino functionality during chemical reactions, allowing selective modification of other parts of the molecule. It is particularly valuable in solid-phase peptide synthesis (SPPS), a method widely employed to produce peptides with high purity and specificity. Additionally, it finds application in the development of chiral c

This compound is primarily used in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. Its tert-butoxycarbonyl (Boc) group protects the amino functionality during chemical reactions, allowing selective modification of other parts of the molecule. It is particularly valuable in solid-phase peptide synthesis (SPPS), a method widely employed to produce peptides with high purity and specificity. Additionally, it finds application in the development of chiral compounds and bioactive molecules, where its stereochemistry plays a crucial role in ensuring the desired biological activity. The hydrate form ensures stability and ease of handling during storage and use in laboratory settings.

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