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

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Reagent Code: #37752
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CAS Number 1445976-44-2

science Other reagents with same CAS 1445976-44-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.32 g/mol
Formula C₁₂H₂₃NO₄
badge Registry Numbers
MDL Number MFCD11973692
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. Its tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amine functionality, preventing unwanted reactions during peptide bond formation. This makes it a valuable intermediate in the production of complex peptide structures, particularly in solid-phase peptide synthesis (SPPS). Additionally, it is employed in the development of bioactive compounds and drug candidates, especially in research targeting therapeutic peptides and enzyme inhibitors. Its chiral nature also makes it useful in asymmetric synthesis for creating enantiomerically pure substances.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,799.00
inventory 100mg
10-20 days ฿1,674.00
inventory 1g
10-20 days ฿8,397.00

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(R)-2-((tert-Butoxycarbonyl)amino)-5-methylhexanoic acid
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This chemical is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. Its tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amine functionality, preventing unwanted reactions during peptide bond formation. This makes it a valuable intermediate in the production of complex peptide structures, particularly in solid-phase peptide synthesis (SPPS). Additionally, it is employed in the development of bioactive compounds and

This chemical is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. Its tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amine functionality, preventing unwanted reactions during peptide bond formation. This makes it a valuable intermediate in the production of complex peptide structures, particularly in solid-phase peptide synthesis (SPPS). Additionally, it is employed in the development of bioactive compounds and drug candidates, especially in research targeting therapeutic peptides and enzyme inhibitors. Its chiral nature also makes it useful in asymmetric synthesis for creating enantiomerically pure substances.

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