(S)-2-((tert-Butoxycarbonyl)amino)heptanoic acid

95%

Reagent Code: #38098
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CAS Number 71066-01-8

science Other reagents with same CAS 71066-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.3200 g/mol
Formula C₁₂H₂₃NO₄
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MDL Number MFCD06659979
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description Product Description

(S)-2-((tert-Butoxycarbonyl)amino)heptanoic acid is primarily used in the synthesis of peptides and peptidomimetics. It serves as a key intermediate in the production of biologically active compounds, particularly in the development of pharmaceuticals. The tert-butoxycarbonyl (Boc) group acts as a protecting group for the amino functionality during peptide synthesis, ensuring selective reactions at other sites. This compound is also utilized in the preparation of chiral molecules, contributing to the creation of enantiomerically pure substances. Its application extends to research in medicinal chemistry, where it aids in the design and optimization of drug candidates with improved efficacy and specificity.

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Test Parameter Specification
Appearance Colorless to Light Yellow Liquid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿774.00

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(S)-2-((tert-Butoxycarbonyl)amino)heptanoic acid
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(S)-2-((tert-Butoxycarbonyl)amino)heptanoic acid is primarily used in the synthesis of peptides and peptidomimetics. It serves as a key intermediate in the production of biologically active compounds, particularly in the development of pharmaceuticals. The tert-butoxycarbonyl (Boc) group acts as a protecting group for the amino functionality during peptide synthesis, ensuring selective reactions at other sites. This compound is also utilized in the preparation of chiral molecules, contributing to the cre

(S)-2-((tert-Butoxycarbonyl)amino)heptanoic acid is primarily used in the synthesis of peptides and peptidomimetics. It serves as a key intermediate in the production of biologically active compounds, particularly in the development of pharmaceuticals. The tert-butoxycarbonyl (Boc) group acts as a protecting group for the amino functionality during peptide synthesis, ensuring selective reactions at other sites. This compound is also utilized in the preparation of chiral molecules, contributing to the creation of enantiomerically pure substances. Its application extends to research in medicinal chemistry, where it aids in the design and optimization of drug candidates with improved efficacy and specificity.

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