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

98%

Reagent Code: #230859
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CAS Number 500789-06-0

science Other reagents with same CAS 500789-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.75 g/mol
Formula C₁₄H₁₈ClNO₄
badge Registry Numbers
MDL Number MFCD03427959
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups allow for selective coupling reactions in peptide-like structures, making it valuable in medicinal chemistry for constructing complex drug candidates. Commonly employed in research settings for optimizing potency and selectivity during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,790.00
inventory 250mg
10-20 days ฿2,690.00
inventory 1g
10-20 days ฿6,680.00
inventory 5g
10-20 days ฿27,080.00
inventory 10g
10-20 days ฿47,080.00
(R)-3-((tert-Butoxycarbonyl)amino)-3-(3-chlorophenyl)propanoic acid
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Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups allow for selective coupling reactions in peptide-like structures, making it valuable in medicinal chemistry for constructing complex drug candidates. Commonly employed in research settings for optimizing potency and selectivity during drug discovery.
Used as a chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups allow for selective coupling reactions in peptide-like structures, making it valuable in medicinal chemistry for constructing complex drug candidates. Commonly employed in research settings for optimizing potency and selectivity during drug discovery.
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