(S)-3-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid

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Reagent Code: #38464
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CAS Number 1956436-56-8

science Other reagents with same CAS 1956436-56-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.30 g/mol
Formula C₁₁H₂₂N₂O₄
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This chemical is primarily used as an intermediate in the synthesis of peptides and other complex organic compounds. It plays a crucial role in the production of pharmaceutical agents, particularly in the development of drugs targeting neurological and metabolic disorders. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides while preventing unwanted side reactions. Additionally, it is utilized in research laboratories for studying enzyme mechanisms and protein interactions, contributing to advancements in biochemistry and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,619.00
inventory 250mg
10-20 days ฿18,531.00
inventory 1g
10-20 days ฿46,332.00

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(S)-3-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid
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This chemical is primarily used as an intermediate in the synthesis of peptides and other complex organic compounds. It plays a crucial role in the production of pharmaceutical agents, particularly in the development of drugs targeting neurological and metabolic disorders. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides while preventing unwanted side reaction

This chemical is primarily used as an intermediate in the synthesis of peptides and other complex organic compounds. It plays a crucial role in the production of pharmaceutical agents, particularly in the development of drugs targeting neurological and metabolic disorders. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides while preventing unwanted side reactions. Additionally, it is utilized in research laboratories for studying enzyme mechanisms and protein interactions, contributing to advancements in biochemistry and medicinal chemistry.

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