(S)-2-Aminohept-6-enoic acid

≥95%

Reagent Code: #38313
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CAS Number 166734-64-1

science Other reagents with same CAS 166734-64-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.18 g/mol
Formula C₇H₁₃NO₂
badge Registry Numbers
MDL Number MFCD06200653
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

(S)-2-Aminohept-6-enoic acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active compounds, including peptides and amino acid derivatives. Its unique structure, featuring both an amino group and an alkene moiety, makes it a valuable building block for constructing complex molecules with potential therapeutic applications. Additionally, it is employed in the development of chiral catalysts and ligands, which are essential in asymmetric synthesis to produce enantiomerically pure substances. This compound is also of interest in biochemical studies, where it is used to explore enzyme mechanisms and protein interactions due to its structural similarity to natural amino acids.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿30,861.00
inventory 100mg
10-20 days ฿15,426.00

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(S)-2-Aminohept-6-enoic acid
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(S)-2-Aminohept-6-enoic acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active compounds, including peptides and amino acid derivatives. Its unique structure, featuring both an amino group and an alkene moiety, makes it a valuable building block for constructing complex molecules with potential therapeutic applications. Additionally, it is employed in the development of chiral catalysts and

(S)-2-Aminohept-6-enoic acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active compounds, including peptides and amino acid derivatives. Its unique structure, featuring both an amino group and an alkene moiety, makes it a valuable building block for constructing complex molecules with potential therapeutic applications. Additionally, it is employed in the development of chiral catalysts and ligands, which are essential in asymmetric synthesis to produce enantiomerically pure substances. This compound is also of interest in biochemical studies, where it is used to explore enzyme mechanisms and protein interactions due to its structural similarity to natural amino acids.

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