3-((tert-Butoxycarbonyl)amino)-3-(3,4-dimethoxyphenyl)propanoic acid

95%

Reagent Code: #104532
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CAS Number 284492-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.36 g/mol
Formula C₁₆H₂₃NO₆
badge Registry Numbers
MDL Number MFCD01931739
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the preparation of peptide derivatives and other bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is commonly employed to safeguard the amino functionality during complex chemical reactions, ensuring selective transformations. The presence of the 3,4-dimethoxyphenyl moiety makes it a valuable intermediate in the synthesis of compounds with potential pharmacological activity, such as those targeting neurological or cardiovascular disorders. Additionally, it serves as a building block in the development of chiral molecules, enabling the creation of enantiomerically pure substances for use in drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,480.00
inventory 1g
10-20 days ฿25,740.00
inventory 250mg
10-20 days ฿12,870.00
3-((tert-Butoxycarbonyl)amino)-3-(3,4-dimethoxyphenyl)propanoic acid
This compound is primarily utilized in organic synthesis, particularly in the preparation of peptide derivatives and other bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is commonly employed to safeguard the amino functionality during complex chemical reactions, ensuring selective transformations. The presence of the 3,4-dimethoxyphenyl moiety makes it a valuable intermediate in the synthesis of compounds with potential pharmacological activity, such as those targeting neurological or cardiovascular disorders. Additionally, it serves as a building block in the development of chiral molecules, enabling the creation of enantiomerically pure substances for use in drug discovery and development.
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