(S)-2-((tert-Butoxycarbonyl)amino)-5-methylhexanoic acid

≥95%

Reagent Code: #38096
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CAS Number 208522-10-5

science Other reagents with same CAS 208522-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.32 g/mol
Formula C₁₂H₂₃NO₄
badge Registry Numbers
MDL Number MFCD00273432
thermostat Physical Properties
Boiling Point 370.1±25.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. This protection is crucial in peptide synthesis to prevent unwanted side reactions. It is particularly valuable in the production of complex peptides and bioactive molecules, where selective deprotection and coupling steps are required. Additionally, it finds application in the development of drug candidates, especially in medicinal chemistry research, where precise control over molecular structure is essential for optimizing biological activity. Its use is common in solid-phase peptide synthesis (SPPS) and other organic synthesis methodologies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿19,710.00
inventory 5g
10-20 days ฿39,420.00

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(S)-2-((tert-Butoxycarbonyl)amino)-5-methylhexanoic acid
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This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. This protection is crucial in peptide synthesis to prevent unwanted side reactions. It is particularly valuable in the production of complex peptides and bioactive molecules, where selective deprotection and coupling steps are required. Additionally, it finds applic

This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. This protection is crucial in peptide synthesis to prevent unwanted side reactions. It is particularly valuable in the production of complex peptides and bioactive molecules, where selective deprotection and coupling steps are required. Additionally, it finds application in the development of drug candidates, especially in medicinal chemistry research, where precise control over molecular structure is essential for optimizing biological activity. Its use is common in solid-phase peptide synthesis (SPPS) and other organic synthesis methodologies.

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