(S)-Benzyl (1-(4-Phenyl-1H-Imidazol-2-Yl)Ethyl)Carbamate

97%

Reagent Code: #237170
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CAS Number 864825-21-8

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.37 g/mol
Formula C₁₉H₁₉N₃O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as a chiral intermediate for developing bioactive molecules, particularly in the production of imidazole-based drugs. Its structure supports the development of compounds with potential antifungal, antiviral, or anticancer activity. The carbamate group allows for selective protection during multi-step synthesis, while the benzyl and phenyl groups enhance lipophilicity, aiding membrane permeability in drug design. Commonly employed in asymmetric synthesis to maintain stereochemical integrity in active pharmaceutical ingredients.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿17,750.00
1g
10-20 days ฿72,460.00
250mg
10-20 days ฿29,520.00
(S)-Benzyl (1-(4-Phenyl-1H-Imidazol-2-Yl)Ethyl)Carbamate
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Used in pharmaceutical synthesis as a chiral intermediate for developing bioactive molecules, particularly in the production of imidazole-based drugs. Its structure supports the development of compounds with potential antifungal, antiviral, or anticancer activity. The carbamate group allows for selective protection during multi-step synthesis, while the benzyl and phenyl groups enhance lipophilicity, aiding membrane permeability in drug design. Commonly employed in asymmetric synthesis to maintain stereo

Used in pharmaceutical synthesis as a chiral intermediate for developing bioactive molecules, particularly in the production of imidazole-based drugs. Its structure supports the development of compounds with potential antifungal, antiviral, or anticancer activity. The carbamate group allows for selective protection during multi-step synthesis, while the benzyl and phenyl groups enhance lipophilicity, aiding membrane permeability in drug design. Commonly employed in asymmetric synthesis to maintain stereochemical integrity in active pharmaceutical ingredients.

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