tert-Butyl 4-(2-ethoxy-2-oxoethyl)piperazine-1-carboxylate

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Reagent Code: #151122
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CAS Number 209667-59-4

science Other reagents with same CAS 209667-59-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.34 g/mol
Formula C₁₃H₂₄N₂O₄
badge Registry Numbers
MDL Number MFCD06795955
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine backbone modifications. Its protected amine group allows selective reactions at other functional sites, making it valuable in multi-step organic syntheses. The ester group can be hydrolyzed to form carboxylic acid derivatives, enabling further conjugation or salt formation. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, metabolic diseases, and infectious conditions. Also utilized in research settings for library generation in medicinal chemistry due to its structural versatility and compatibility with various coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,310.00
inventory 250mg
10-20 days ฿2,610.00
inventory 1g
10-20 days ฿3,570.00

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tert-Butyl 4-(2-ethoxy-2-oxoethyl)piperazine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine backbone modifications. Its protected amine group allows selective reactions at other functional sites, making it valuable in multi-step organic syntheses. The ester group can be hydrolyzed to form carboxylic acid derivatives, enabling further conjugation or salt formation. Commonly employed in the preparation of drug candidates targeting central nervous

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) that require piperazine backbone modifications. Its protected amine group allows selective reactions at other functional sites, making it valuable in multi-step organic syntheses. The ester group can be hydrolyzed to form carboxylic acid derivatives, enabling further conjugation or salt formation. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, metabolic diseases, and infectious conditions. Also utilized in research settings for library generation in medicinal chemistry due to its structural versatility and compatibility with various coupling reactions.

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