(R)-2-((tert-Butoxycarbonyl)amino)-3-(3,5-dichlorophenyl)propanoic acid

95%

Reagent Code: #37459
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CAS Number 1212983-95-3

science Other reagents with same CAS 1212983-95-3

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Weight 334.1951 g/mol
Formula C₁₄H₁₇Cl₂NO₄
badge Registry Numbers
MDL Number MFCD07372032
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic applications. It serves as a key building block in the preparation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a dichlorophenyl moiety, makes it valuable in peptide synthesis and medicinal chemistry research. The compound is often employed in the creation of drug candidates for conditions like inflammation, central nervous system disorders, or infectious diseases, where precise molecular design is critical for efficacy and selectivity. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing therapeutic outcomes and reducing side effects.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,250.00

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(R)-2-((tert-Butoxycarbonyl)amino)-3-(3,5-dichlorophenyl)propanoic acid
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic applications. It serves as a key building block in the preparation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a dichlorophenyl moiety, makes it valuable in peptide synthesis and medicinal chemistry

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic applications. It serves as a key building block in the preparation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a dichlorophenyl moiety, makes it valuable in peptide synthesis and medicinal chemistry research. The compound is often employed in the creation of drug candidates for conditions like inflammation, central nervous system disorders, or infectious diseases, where precise molecular design is critical for efficacy and selectivity. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing therapeutic outcomes and reducing side effects.

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