(R)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid hydrate

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Reagent Code: #97472
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CAS Number 200937-17-3

science Other reagents with same CAS 200937-17-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.3 g/mol
Formula C₁₁H₂₃NO₅
thermostat Physical Properties
Melting Point 85-87°C
Boiling Point 356°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in peptide synthesis as a building block. It serves as a protected amino acid, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during the synthesis process. This allows for selective reactions at other sites of the molecule without interference. It is particularly useful in creating complex peptides for pharmaceutical research, enabling the development of drugs targeting various diseases. Additionally, its chiral nature makes it valuable in producing enantiomerically pure compounds, which are critical in drug design to ensure specificity and reduce side effects.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to very pale yellow crystal or powder
Purity 96.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿420.00
inventory 100g
10-20 days ฿5,160.00
inventory 25g
10-20 days ฿1,310.00
inventory 1g
10-20 days ฿300.00
inventory 500g
10-20 days ฿24,680.00
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(R)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid hydrate
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This compound is primarily used in peptide synthesis as a building block. It serves as a protected amino acid, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during the synthesis process. This allows for selective reactions at other sites of the molecule without interference. It is particularly useful in creating complex peptides for pharmaceutical research, enabling the development of drugs targeting various diseases. Additionally, its chiral nature makes it valuable in producing enantiomerically pure compounds, which are critical in drug design to ensure specificity and reduce side effects.
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