(R)-5-Benzyl-2,2,3-Trimethylimidazolidin-4-One 2,2,2-Trifluoroacetate

97%

Reagent Code: #231609
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CAS Number 685128-78-3

science Other reagents with same CAS 685128-78-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.32 g/mol
Formula C₁₅H₁₉F₃N₂O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its rigid imidazolidinone structure helps control stereochemistry during key bond-forming reactions, such as aldol or alkylation reactions. The trifluoroacetate salt enhances solubility and stability in organic solvents, making it suitable for use in multi-step synthetic routes. Commonly employed in the development of active pharmaceutical ingredients (APIs) where stereochemical precision is critical for biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,940.00
(R)-5-Benzyl-2,2,3-Trimethylimidazolidin-4-One 2,2,2-Trifluoroacetate
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Used as a chiral auxiliary in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its rigid imidazolidinone structure helps control stereochemistry during key bond-forming reactions, such as aldol or alkylation reactions. The trifluoroacetate salt enhances solubility and stability in organic solvents, making it suitable for use in multi-step synthetic routes. Commonly employed in the development of active pharmaceutical ingredients (AP

Used as a chiral auxiliary in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its rigid imidazolidinone structure helps control stereochemistry during key bond-forming reactions, such as aldol or alkylation reactions. The trifluoroacetate salt enhances solubility and stability in organic solvents, making it suitable for use in multi-step synthetic routes. Commonly employed in the development of active pharmaceutical ingredients (APIs) where stereochemical precision is critical for biological activity.

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