(R)-3-(Boc-amino)-4-(3,4-dichlorophenyl)butyricacid

95%

Reagent Code: #230009
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CAS Number 269396-56-7

science Other reagents with same CAS 269396-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.22 g/mol
Formula C₁₅H₁₉Cl₂NO₄
badge Registry Numbers
MDL Number MFCD01860949
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other biologically active compounds. Its chiral center and functional groups make it valuable in asymmetric synthesis, enabling the construction of complex molecules with high enantioselectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in central nervous system agents and enzyme inhibitors. The Boc-protected amine allows for controlled deprotection and coupling in peptide-like frameworks, facilitating modular drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,100.00
inventory 250mg
10-20 days ฿1,750.00
inventory 1g
10-20 days ฿5,380.00
inventory 5g
10-20 days ฿25,960.00

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(R)-3-(Boc-amino)-4-(3,4-dichlorophenyl)butyricacid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other biologically active compounds. Its chiral center and functional groups make it valuable in asymmetric synthesis, enabling the construction of complex molecules with high enantioselectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in central nervous system agents and enzyme inhibitors. The Boc-protected amine allows for controlled

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other biologically active compounds. Its chiral center and functional groups make it valuable in asymmetric synthesis, enabling the construction of complex molecules with high enantioselectivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in central nervous system agents and enzyme inhibitors. The Boc-protected amine allows for controlled deprotection and coupling in peptide-like frameworks, facilitating modular drug design.

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