(R)-Tert-Butyl 2-(1-(4-(Ethoxycarbonyl)Phenyl)Ethyl)Hydrazinecarboxylate

95%

Reagent Code: #231569
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CAS Number 870822-90-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.37 g/mol
Formula C₁₆H₂₄N₂O₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as a chiral hydrazine derivative, particularly in the preparation of bioactive molecules requiring stereochemical control. Its protected hydrazine functionality allows for selective reactions in multi-step organic syntheses, especially in the development of enzyme inhibitors and receptor modulators. The ethoxycarbonyl-containing aryl group enhances solubility and can act as a prodrug moiety in medicinal chemistry applications. Commonly employed in asymmetric synthesis due to the (R)-configuration, enabling the formation of enantiomerically pure intermediates for drug candidates targeting central nervous system disorders and metabolic diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,930.00
inventory 250mg
10-20 days ฿21,550.00
inventory 1g
10-20 days ฿52,890.00
(R)-Tert-Butyl 2-(1-(4-(Ethoxycarbonyl)Phenyl)Ethyl)Hydrazinecarboxylate
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Used in pharmaceutical synthesis as a chiral hydrazine derivative, particularly in the preparation of bioactive molecules requiring stereochemical control. Its protected hydrazine functionality allows for selective reactions in multi-step organic syntheses, especially in the development of enzyme inhibitors and receptor modulators. The ethoxycarbonyl-containing aryl group enhances solubility and can act as a prodrug moiety in medicinal chemistry applications. Commonly employed in asymmetric synthesis due

Used in pharmaceutical synthesis as a chiral hydrazine derivative, particularly in the preparation of bioactive molecules requiring stereochemical control. Its protected hydrazine functionality allows for selective reactions in multi-step organic syntheses, especially in the development of enzyme inhibitors and receptor modulators. The ethoxycarbonyl-containing aryl group enhances solubility and can act as a prodrug moiety in medicinal chemistry applications. Commonly employed in asymmetric synthesis due to the (R)-configuration, enabling the formation of enantiomerically pure intermediates for drug candidates targeting central nervous system disorders and metabolic diseases.

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