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

95%

Reagent Code: #104531
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CAS Number 193633-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.20 g/mol
Formula C₁₄H₁₇Cl₂NO₄
badge Registry Numbers
MDL Number MFCD02090707
thermostat Physical Properties
Boiling Point 475.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.321±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting neurological disorders, such as epilepsy and anxiety, due to its structural compatibility with biologically active molecules. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during peptide synthesis, making it valuable in the creation of complex organic molecules. Additionally, it is utilized in research settings for the study of enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. Its dichlorophenyl moiety contributes to its potential use in the design of compounds with enhanced biological activity and specificity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,590.00
inventory 1g
10-20 days ฿11,529.00
inventory 250mg
10-20 days ฿7,659.00
3-((tert-Butoxycarbonyl)amino)-3-(3,4-dichlorophenyl)propanoic acid
This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting neurological disorders, such as epilepsy and anxiety, due to its structural compatibility with biologically active molecules. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during peptide synthesis, making it valuable in the creation of complex organic molecules. Additionally, it is utilized in research settings for the study of enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. Its dichlorophenyl moiety contributes to its potential use in the design of compounds with enhanced biological activity and specificity.
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