Benzyl (2S)-2-aminohexanoate toluene-4-sulfonic acid salt

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Reagent Code: #60678
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CAS Number 63219-55-6

science Other reagents with same CAS 63219-55-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.51 g/mol
Formula C₂₀H₂₇NO₅S
badge Registry Numbers
MDL Number MFCD27957345
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an amino group and a benzyl ester, makes it suitable for peptide synthesis and modification processes. It is often employed in the preparation of enantiomerically pure compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Additionally, it serves as a chiral building block in organic chemistry, enabling the creation of complex molecules with high stereochemical precision. Its toluene-4-sulfonic acid salt form enhances stability and solubility, facilitating its use in controlled reactions and formulations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿19,800.00

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Benzyl (2S)-2-aminohexanoate toluene-4-sulfonic acid salt
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an amino group and a benzyl ester, makes it suitable for peptide synthesis and modification processes. It is often employed in the preparation of enantiomerically pure compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Additionally, it serves as a chiral building block

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an amino group and a benzyl ester, makes it suitable for peptide synthesis and modification processes. It is often employed in the preparation of enantiomerically pure compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Additionally, it serves as a chiral building block in organic chemistry, enabling the creation of complex molecules with high stereochemical precision. Its toluene-4-sulfonic acid salt form enhances stability and solubility, facilitating its use in controlled reactions and formulations.

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