(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid

≥95%

Reagent Code: #38079
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CAS Number 142186-36-5

science Other reagents with same CAS 142186-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.27 g/mol
Formula C₁₃H₁₆FNO₄
badge Registry Numbers
MDL Number MFCD01320862
thermostat Physical Properties
Boiling Point 408.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly significant in the production of chiral drugs, where its stereochemistry plays a crucial role in ensuring the desired biological activity. The presence of the 4-fluorophenyl group enhances its application in the development of compounds with specific receptor-binding properties, often found in medications targeting neurological or cardiovascular conditions. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes, making it valuable for constructing complex molecules with precision. Its applications extend to research and development, where it is used to explore new therapeutic agents and optimize drug efficacy.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿31,410.00
inventory 250mg
10-20 days ฿2,556.00
inventory 5g
10-20 days ฿19,242.00
inventory 1g
10-20 days ฿6,399.00

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(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly significant in the production of chiral drugs, where its stereochemistry plays a crucial role in ensuring the desired biological activity. The presence of the 4-fluorophenyl group enhances its application in the development of compounds with specific receptor-binding properties, often found in medications targeting neurological or cardiovascular conditions. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes, making it valuable for constructing complex molecules with precision. Its applications extend to research and development, where it is used to explore new therapeutic agents and optimize drug efficacy.
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