(S)-3-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid

≥97%

Reagent Code: #38381
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CAS Number 179412-79-4

science Other reagents with same CAS 179412-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.28 g/mol
Formula C₁₁H₂₁NO₄
badge Registry Numbers
MDL Number MFCD01076232
thermostat Physical Properties
Boiling Point 360.4±25.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step organic syntheses, particularly in the production of complex molecules like peptide-based drugs. Its application is common in medicinal chemistry for designing and developing bioactive compounds, including enzyme inhibitors and receptor modulators. Additionally, it is employed in research settings to study peptide structure-activity relationships and to create custom peptides for biochemical studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,338.00
inventory 250mg
10-20 days ฿1,737.00
inventory 5g
10-20 days ฿13,860.00
inventory 100mg
10-20 days ฿1,161.00

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(S)-3-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid
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This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step organic syntheses, particularly in the production of complex molecules like peptide-based drugs. Its application is common in medicinal chemistry for designing and developing bioactive compounds, including enzyme inhi

This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step organic syntheses, particularly in the production of complex molecules like peptide-based drugs. Its application is common in medicinal chemistry for designing and developing bioactive compounds, including enzyme inhibitors and receptor modulators. Additionally, it is employed in research settings to study peptide structure-activity relationships and to create custom peptides for biochemical studies.

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