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

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Reagent Code: #153836
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CAS Number 1993394-57-2

science Other reagents with same CAS 1993394-57-2

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Weight 411.41 g/mol
Formula C₂₁H₂₁N₃O₆
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Storage Room temperature

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Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of imidazole-based drugs. Shows potential in the creation of antifungal, antiviral, and anticancer agents due to the imidazole core’s affinity for biological targets. The benzyl carbamate group acts as a protecting group in peptide synthesis, enabling selective reactions in multi-step organic syntheses. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates. Soluble forms like the oxalate salt aid in improving bioavailability during preclinical testing.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,530.00

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Benzyl (S)-(1-(4-Phenyl-1H-Imidazol-2-Yl)Ethyl)Carbamate Oxalate
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Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of imidazole-based drugs. Shows potential in the creation of antifungal, antiviral, and anticancer agents due to the imidazole core’s affinity for biological targets. The benzyl carbamate group acts as a protecting group in peptide synthesis, enabling selective reactions in multi-step organic syntheses. Also employed in medicinal chemistry for structure-activity relationship (SAR) stud

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of imidazole-based drugs. Shows potential in the creation of antifungal, antiviral, and anticancer agents due to the imidazole core’s affinity for biological targets. The benzyl carbamate group acts as a protecting group in peptide synthesis, enabling selective reactions in multi-step organic syntheses. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates. Soluble forms like the oxalate salt aid in improving bioavailability during preclinical testing.

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