(R)-3-((tert-Butoxycarbonyl)amino)-3-(2-chlorophenyl)propanoic acid

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Reagent Code: #104252
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CAS Number 500789-05-9

science Other reagents with same CAS 500789-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.75 g/mol
Formula C₁₄H₁₈ClNO₄
badge Registry Numbers
MDL Number MFCD03427958
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it valuable for constructing chiral compounds, which are essential in the production of enantiomerically pure drugs. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molecule. Additionally, the presence of the chlorophenyl group can enhance binding affinity to specific biological targets, making it useful in the design of receptor-specific drugs. Its application is often seen in the development of therapeutic agents targeting neurological disorders, cardiovascular diseases, or other conditions where chiral specificity is critical.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,870.00
inventory 100mg
10-20 days ฿2,610.00
inventory 1g
10-20 days ฿9,720.00

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(R)-3-((tert-Butoxycarbonyl)amino)-3-(2-chlorophenyl)propanoic acid
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it valuable for constructing chiral compounds, which are essential in the production of enantiomerically pure drugs. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molecule.

This compound is primarily utilized in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it valuable for constructing chiral compounds, which are essential in the production of enantiomerically pure drugs. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molecule. Additionally, the presence of the chlorophenyl group can enhance binding affinity to specific biological targets, making it useful in the design of receptor-specific drugs. Its application is often seen in the development of therapeutic agents targeting neurological disorders, cardiovascular diseases, or other conditions where chiral specificity is critical.

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