tert-Butyl (S)-2-(2,6-Dichlorophenyl)-5-oxo-3-[(S)-1-phenylethyl]imidazolidine-1-carboxylate

≥98%(LC&N)

Reagent Code: #149409
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CAS Number 1149765-08-1

science Other reagents with same CAS 1149765-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 435.35 g/mol
Formula C₂₂H₂₄Cl₂N₂O₃
badge Registry Numbers
MDL Number MFCD30187601
thermostat Physical Properties
Melting Point 100 °C
inventory_2 Storage & Handling
Storage 2-8℃, stored in inert gas

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of enantiomerically pure pharmaceuticals. Its rigid imidazolidine backbone and stereodefined centers make it valuable in asymmetric synthesis, where it can serve as a building block for protease inhibitors or receptor modulators. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during peptide-like chain elongation. Commonly employed in medicinal chemistry for optimizing stereochemistry in drug candidates targeting central nervous system disorders and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,760.00

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tert-Butyl (S)-2-(2,6-Dichlorophenyl)-5-oxo-3-[(S)-1-phenylethyl]imidazolidine-1-carboxylate
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Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of enantiomerically pure pharmaceuticals. Its rigid imidazolidine backbone and stereodefined centers make it valuable in asymmetric synthesis, where it can serve as a building block for protease inhibitors or receptor modulators. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during peptide-like chain elongation. Commonly employed in medicinal chemistry for op

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of enantiomerically pure pharmaceuticals. Its rigid imidazolidine backbone and stereodefined centers make it valuable in asymmetric synthesis, where it can serve as a building block for protease inhibitors or receptor modulators. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during peptide-like chain elongation. Commonly employed in medicinal chemistry for optimizing stereochemistry in drug candidates targeting central nervous system disorders and inflammatory diseases.

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